| 71120160 |
71120183 |
X |
- |
26472758 |
Jiyoye |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-1.218659400630811 |
[178] |
[57] |
-7 |
hSpCas9 |
negative selection |
98111 |
71126379 |
71126402 |
X |
- |
26472758 |
Jiyoye |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-2.575546627062291 |
[165] |
[20] |
-9 |
hSpCas9 |
negative selection |
98112 |
71125361 |
71125384 |
X |
+ |
26472758 |
Jiyoye |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-0.981095208210185 |
[88] |
[33] |
-6 |
hSpCas9 |
negative selection |
98113 |
71132900 |
71132923 |
X |
+ |
26472758 |
Jiyoye |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-5.8022779841230765 |
[73] |
[0] |
-9 |
hSpCas9 |
negative selection |
98114 |
71134388 |
71134411 |
X |
+ |
26472758 |
Jiyoye |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-2.722107635439093 |
[34] |
[3] |
-9 |
hSpCas9 |
negative selection |
98115 |
71119757 |
71119780 |
X |
+ |
26472758 |
Jiyoye |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-2.955394697878835 |
[71] |
[6] |
-9 |
hSpCas9 |
negative selection |
98116 |
71123631 |
71123654 |
X |
- |
26472758 |
Jiyoye |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.1333929998568295 |
[63] |
[21] |
-6 |
hSpCas9 |
negative selection |
98117 |
71124305 |
71124328 |
X |
- |
26472758 |
Jiyoye |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
-0.1058942007334972 |
[136] |
[95] |
0 |
hSpCas9 |
negative selection |
98118 |
71125083 |
71125106 |
X |
- |
26472758 |
Jiyoye |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-1.762749619936439 |
[71] |
[15] |
-8 |
hSpCas9 |
negative selection |
98119 |
71125377 |
71125400 |
X |
- |
26472758 |
Jiyoye |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-4.293264336635219 |
[25] |
[0] |
-9 |
hSpCas9 |
negative selection |
98120 |
71120160 |
71120183 |
X |
- |
26472758 |
KBM7 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.2206700488175435 |
[427,421] |
[60,26] |
-8 |
hSpCas9 |
negative selection |
289229 |
71126379 |
71126402 |
X |
- |
26472758 |
KBM7 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.6683402725866325 |
[621,492] |
[64,96] |
-8 |
hSpCas9 |
negative selection |
289230 |
71125361 |
71125384 |
X |
+ |
26472758 |
KBM7 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-1.1528841938070542 |
[806,643] |
[295,23] |
-7 |
hSpCas9 |
negative selection |
289231 |
71132900 |
71132923 |
X |
+ |
26472758 |
KBM7 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-2.474874689399314 |
[589,271] |
[20,47] |
-9 |
hSpCas9 |
negative selection |
289232 |
71134388 |
71134411 |
X |
+ |
26472758 |
KBM7 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-1.303009186483561 |
[255,210] |
[57,31] |
-7 |
hSpCas9 |
negative selection |
289233 |
71119757 |
71119780 |
X |
+ |
26472758 |
KBM7 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.1115284481817906 |
[254,294] |
[77,44] |
-7 |
hSpCas9 |
negative selection |
289234 |
71123631 |
71123654 |
X |
- |
26472758 |
KBM7 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-0.3243150922488285 |
[181,93] |
[61,39] |
-3 |
hSpCas9 |
negative selection |
289235 |
71124305 |
71124328 |
X |
- |
26472758 |
KBM7 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.7671210777731259 |
[438,352] |
[363,270] |
8 |
hSpCas9 |
negative selection |
289236 |
71125083 |
71125106 |
X |
- |
26472758 |
KBM7 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
0.4697377047465455 |
[308,276] |
[168,209] |
5 |
hSpCas9 |
negative selection |
289237 |
71125377 |
71125400 |
X |
- |
26472758 |
KBM7 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-0.4915847947622134 |
[83,102] |
[45,18] |
-4 |
hSpCas9 |
negative selection |
289238 |
71120160 |
71120183 |
X |
- |
26472758 |
Raji |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-0.8816453468053974 |
[261] |
[32] |
-6 |
hSpCas9 |
negative selection |
480347 |
71126379 |
71126402 |
X |
- |
26472758 |
Raji |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.6999713866840045 |
[293] |
[20] |
-8 |
hSpCas9 |
negative selection |
480348 |
71125361 |
71125384 |
X |
+ |
26472758 |
Raji |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-2.6142415126581207 |
[342] |
[12] |
-9 |
hSpCas9 |
negative selection |
480349 |
71132900 |
71132923 |
X |
+ |
26472758 |
Raji |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-1.6722263962011006 |
[205] |
[14] |
-8 |
hSpCas9 |
negative selection |
480350 |
71134388 |
71134411 |
X |
+ |
26472758 |
Raji |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-2.0423635841310825 |
[70] |
[3] |
-8 |
hSpCas9 |
negative selection |
480351 |
71119757 |
71119780 |
X |
+ |
26472758 |
Raji |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.1150088859628484 |
[223] |
[23] |
-7 |
hSpCas9 |
negative selection |
480352 |
71123631 |
71123654 |
X |
- |
26472758 |
Raji |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.140543978069986 |
[75] |
[7] |
-7 |
hSpCas9 |
negative selection |
480353 |
71124305 |
71124328 |
X |
- |
26472758 |
Raji |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.43658486517313955 |
[276] |
[86] |
4 |
hSpCas9 |
negative selection |
480354 |
71125083 |
71125106 |
X |
- |
26472758 |
Raji |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
0.3833569969148913 |
[184] |
[55] |
3 |
hSpCas9 |
negative selection |
480355 |
71125377 |
71125400 |
X |
- |
26472758 |
Raji |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-1.1405439780699864 |
[18] |
[1] |
-7 |
hSpCas9 |
negative selection |
480356 |
71120160 |
71120183 |
X |
- |
26472758 |
K562 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-3.547395343495379 |
[276] |
[19] |
-8 |
hSpCas9 |
negative selection |
671465 |
71126379 |
71126402 |
X |
- |
26472758 |
K562 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-2.480316577714347 |
[508] |
[76] |
-8 |
hSpCas9 |
negative selection |
671466 |
71125361 |
71125384 |
X |
+ |
26472758 |
K562 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-3.9680308904224226 |
[481] |
[25] |
-9 |
hSpCas9 |
negative selection |
671467 |
71132900 |
71132923 |
X |
+ |
26472758 |
K562 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-3.0979734697806314 |
[283] |
[27] |
-8 |
hSpCas9 |
negative selection |
671468 |
71134388 |
71134411 |
X |
+ |
26472758 |
K562 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-2.618699465913166 |
[210] |
[28] |
-8 |
hSpCas9 |
negative selection |
671469 |
71119757 |
71119780 |
X |
+ |
26472758 |
K562 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.2701544451633116 |
[179] |
[62] |
-6 |
hSpCas9 |
negative selection |
671470 |
71123631 |
71123654 |
X |
- |
26472758 |
K562 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.7004397181410922 |
[153] |
[39] |
-7 |
hSpCas9 |
negative selection |
671471 |
71124305 |
71124328 |
X |
- |
26472758 |
K562 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
1.3929944089153259 |
[294] |
[653] |
9 |
hSpCas9 |
negative selection |
671472 |
71125083 |
71125106 |
X |
- |
26472758 |
K562 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-0.8800286432580418 |
[241] |
[110] |
-5 |
hSpCas9 |
negative selection |
671473 |
71125377 |
71125400 |
X |
- |
26472758 |
K562 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-4.799975391692007 |
[65] |
[1] |
-9 |
hSpCas9 |
negative selection |
671474 |
71118815 |
71118838 |
X |
- |
26627737 |
DLD1 |
viability |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-5.1348379252292915 |
[256] |
[4,0,0] |
-9 |
hSpCas9 |
negative selection |
846380 |
71119735 |
71119758 |
X |
- |
26627737 |
DLD1 |
viability |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.5215320995851793 |
[1222] |
[26,28,131] |
-9 |
hSpCas9 |
negative selection |
846381 |
71120087 |
71120110 |
X |
- |
26627737 |
DLD1 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.6348587281246705 |
[242] |
[11,60,4] |
-8 |
hSpCas9 |
negative selection |
846382 |
71121019 |
71121042 |
X |
+ |
26627737 |
DLD1 |
viability |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.14216457993880366 |
[645] |
[393,150,133] |
1 |
hSpCas9 |
negative selection |
846383 |
71121386 |
71121409 |
X |
- |
26627737 |
DLD1 |
viability |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-3.3532093591004273 |
[593] |
[28,0,22] |
-9 |
hSpCas9 |
negative selection |
846384 |
71121596 |
71121619 |
X |
- |
26627737 |
DLD1 |
viability |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-5.217159232379825 |
[118] |
[0,0,0] |
-9 |
hSpCas9 |
negative selection |
846385 |
71118815 |
71118838 |
X |
- |
26627737 |
GBM cells |
viability after 5 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-2.271011126556627 |
[125] |
[9,17] |
-9 |
hSpCas9 |
negative selection |
928695 |
71119735 |
71119758 |
X |
- |
26627737 |
GBM cells |
viability after 5 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.221303207301706 |
[812] |
[60,125] |
-9 |
hSpCas9 |
negative selection |
928696 |
71120087 |
71120110 |
X |
- |
26627737 |
GBM cells |
viability after 5 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.7276424477358566 |
[133] |
[85,151] |
8 |
hSpCas9 |
negative selection |
928697 |
71121019 |
71121042 |
X |
+ |
26627737 |
GBM cells |
viability after 5 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.619391346263323 |
[263] |
[224,209] |
8 |
hSpCas9 |
negative selection |
928698 |
71121386 |
71121409 |
X |
- |
26627737 |
GBM cells |
viability after 5 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-1.6264391366973154 |
[402] |
[99,39] |
-9 |
hSpCas9 |
negative selection |
928699 |
71121596 |
71121619 |
X |
- |
26627737 |
GBM cells |
viability after 5 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-1.202015033965095 |
[147] |
[43,24] |
-9 |
hSpCas9 |
negative selection |
928700 |
71118815 |
71118838 |
X |
- |
26627737 |
GBM cells |
viability after 13 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-3.1018221135634807 |
[125] |
[2,11] |
-9 |
hSpCas9 |
negative selection |
1011010 |
71119735 |
71119758 |
X |
- |
26627737 |
GBM cells |
viability after 13 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-3.6433520390883256 |
[812] |
[15,50] |
-9 |
hSpCas9 |
negative selection |
1011011 |
71120087 |
71120110 |
X |
- |
26627737 |
GBM cells |
viability after 13 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.9209209713255438 |
[133] |
[135,138] |
9 |
hSpCas9 |
negative selection |
1011012 |
71121019 |
71121042 |
X |
+ |
26627737 |
GBM cells |
viability after 13 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.41918653219246615 |
[263] |
[158,217] |
5 |
hSpCas9 |
negative selection |
1011013 |
71121386 |
71121409 |
X |
- |
26627737 |
GBM cells |
viability after 13 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-1.9632849304737443 |
[402] |
[65,47] |
-9 |
hSpCas9 |
negative selection |
1011014 |
71121596 |
71121619 |
X |
- |
26627737 |
GBM cells |
viability after 13 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-3.623650194745824 |
[147] |
[0,10] |
-9 |
hSpCas9 |
negative selection |
1011015 |
71118815 |
71118838 |
X |
- |
26627737 |
GBM cells |
viability after 21 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-5.097046623884258 |
[125] |
[1,1] |
-9 |
hSpCas9 |
negative selection |
1093325 |
71119735 |
71119758 |
X |
- |
26627737 |
GBM cells |
viability after 21 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-4.764017284650557 |
[812] |
[21,10] |
-9 |
hSpCas9 |
negative selection |
1093326 |
71120087 |
71120110 |
X |
- |
26627737 |
GBM cells |
viability after 21 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.18210375598100637 |
[133] |
[71,56] |
-2 |
hSpCas9 |
negative selection |
1093327 |
71121019 |
71121042 |
X |
+ |
26627737 |
GBM cells |
viability after 21 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
-0.09269845718617074 |
[263] |
[157,112] |
-1 |
hSpCas9 |
negative selection |
1093328 |
71121386 |
71121409 |
X |
- |
26627737 |
GBM cells |
viability after 21 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-3.658001003264075 |
[402] |
[20,13] |
-9 |
hSpCas9 |
negative selection |
1093329 |
71121596 |
71121619 |
X |
- |
26627737 |
GBM cells |
viability after 21 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-3.7657907268417765 |
[147] |
[7,3] |
-9 |
hSpCas9 |
negative selection |
1093330 |
71118815 |
71118838 |
X |
- |
26627737 |
RPE1 |
viability after 9 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.8612412830122929 |
[588] |
[42,176] |
-6 |
hSpCas9 |
negative selection |
1175640 |
71119735 |
71119758 |
X |
- |
26627737 |
RPE1 |
viability after 9 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-1.4887263483706326 |
[2763] |
[227,411] |
-8 |
hSpCas9 |
negative selection |
1175641 |
71120087 |
71120110 |
X |
- |
26627737 |
RPE1 |
viability after 9 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.8220023655401157 |
[517] |
[82,102] |
-5 |
hSpCas9 |
negative selection |
1175642 |
71121019 |
71121042 |
X |
+ |
26627737 |
RPE1 |
viability after 9 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.2059292169473512 |
[975] |
[703,705] |
7 |
hSpCas9 |
negative selection |
1175643 |
71121386 |
71121409 |
X |
- |
26627737 |
RPE1 |
viability after 9 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-1.6938892892246495 |
[1327] |
[69,203] |
-8 |
hSpCas9 |
negative selection |
1175644 |
71121596 |
71121619 |
X |
- |
26627737 |
RPE1 |
viability after 9 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-5.192098772618111 |
[971] |
[13,0] |
-9 |
hSpCas9 |
negative selection |
1175645 |
71118815 |
71118838 |
X |
- |
26627737 |
RPE1 |
viability after 12 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.9191029512229223 |
[588] |
[4,166] |
-6 |
hSpCas9 |
negative selection |
1257955 |
71119735 |
71119758 |
X |
- |
26627737 |
RPE1 |
viability after 12 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.2811995442614688 |
[2763] |
[110,196] |
-8 |
hSpCas9 |
negative selection |
1257956 |
71120087 |
71120110 |
X |
- |
26627737 |
RPE1 |
viability after 12 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.1072346162068536 |
[517] |
[33,96] |
-6 |
hSpCas9 |
negative selection |
1257957 |
71121019 |
71121042 |
X |
+ |
26627737 |
RPE1 |
viability after 12 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.8730373351166314 |
[975] |
[437,524] |
5 |
hSpCas9 |
negative selection |
1257958 |
71121386 |
71121409 |
X |
- |
26627737 |
RPE1 |
viability after 12 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-2.579614259551645 |
[1327] |
[65,52] |
-9 |
hSpCas9 |
negative selection |
1257959 |
71121596 |
71121619 |
X |
- |
26627737 |
RPE1 |
viability after 12 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-4.565527071609529 |
[971] |
[11,9] |
-9 |
hSpCas9 |
negative selection |
1257960 |
71118815 |
71118838 |
X |
- |
26627737 |
RPE1 |
viability after 15 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-1.8632132880127734 |
[588] |
[0,88] |
-8 |
hSpCas9 |
negative selection |
1340270 |
71119735 |
71119758 |
X |
- |
26627737 |
RPE1 |
viability after 15 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.294670224276381 |
[2763] |
[82,232] |
-8 |
hSpCas9 |
negative selection |
1340271 |
71120087 |
71120110 |
X |
- |
26627737 |
RPE1 |
viability after 15 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-2.5428714482556023 |
[517] |
[16,32] |
-8 |
hSpCas9 |
negative selection |
1340272 |
71121019 |
71121042 |
X |
+ |
26627737 |
RPE1 |
viability after 15 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.47558298212732003 |
[975] |
[445,323] |
3 |
hSpCas9 |
negative selection |
1340273 |
71121386 |
71121409 |
X |
- |
26627737 |
RPE1 |
viability after 15 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-3.6703156124694827 |
[1327] |
[0,56] |
-9 |
hSpCas9 |
negative selection |
1340274 |
71121596 |
71121619 |
X |
- |
26627737 |
RPE1 |
viability after 15 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-5.080394554384171 |
[971] |
[0,14] |
-9 |
hSpCas9 |
negative selection |
1340275 |
71118815 |
71118838 |
X |
- |
26627737 |
RPE1 |
viability after 18 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-2.0560959343938983 |
[588] |
[0,77] |
-8 |
hSpCas9 |
negative selection |
1422585 |
71119735 |
71119758 |
X |
- |
26627737 |
RPE1 |
viability after 18 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.533025127565062 |
[2763] |
[66,194] |
-8 |
hSpCas9 |
negative selection |
1422586 |
71120087 |
71120110 |
X |
- |
26627737 |
RPE1 |
viability after 18 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-3.024076006548839 |
[517] |
[7,26] |
-9 |
hSpCas9 |
negative selection |
1422587 |
71121019 |
71121042 |
X |
+ |
26627737 |
RPE1 |
viability after 18 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.6763799551398029 |
[975] |
[520,313] |
4 |
hSpCas9 |
negative selection |
1422588 |
71121386 |
71121409 |
X |
- |
26627737 |
RPE1 |
viability after 18 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-1.5389706910754755 |
[1327] |
[30,221] |
-7 |
hSpCas9 |
negative selection |
1422589 |
71121596 |
71121619 |
X |
- |
26627737 |
RPE1 |
viability after 18 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-8.035144243505037 |
[971] |
[0,0] |
-9 |
hSpCas9 |
negative selection |
1422590 |
71118815 |
71118838 |
X |
- |
26627737 |
HeLa |
viability after 8 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
0.6251970704987763 |
[148] |
[189,76,55] |
5 |
hSpCas9 |
negative selection |
1504900 |
71119735 |
71119758 |
X |
- |
26627737 |
HeLa |
viability after 8 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
0.13534316758351883 |
[1156] |
[511,645,495] |
1 |
hSpCas9 |
negative selection |
1504901 |
71120087 |
71120110 |
X |
- |
26627737 |
HeLa |
viability after 8 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
1.0393726497120197 |
[149] |
[136,189,79] |
7 |
hSpCas9 |
negative selection |
1504902 |
71121019 |
71121042 |
X |
+ |
26627737 |
HeLa |
viability after 8 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.4200922352543102 |
[289] |
[619,173,284] |
8 |
hSpCas9 |
negative selection |
1504903 |
71121386 |
71121409 |
X |
- |
26627737 |
HeLa |
viability after 8 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
0.22877212438046904 |
[406] |
[267,309,67] |
2 |
hSpCas9 |
negative selection |
1504904 |
71121596 |
71121619 |
X |
- |
26627737 |
HeLa |
viability after 8 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-1.6948174209579996 |
[404] |
[108,21,44] |
-9 |
hSpCas9 |
negative selection |
1504905 |
71118815 |
71118838 |
X |
- |
26627737 |
HeLa |
viability after 12 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
0.21622169522781198 |
[148] |
[120,52,43] |
2 |
hSpCas9 |
negative selection |
1587215 |
71119735 |
71119758 |
X |
- |
26627737 |
HeLa |
viability after 12 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
0.1292870449764827 |
[1156] |
[545,471,556] |
1 |
hSpCas9 |
negative selection |
1587216 |
71120087 |
71120110 |
X |
- |
26627737 |
HeLa |
viability after 12 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
1.0505483933182815 |
[149] |
[142,105,138] |
7 |
hSpCas9 |
negative selection |
1587217 |
71121019 |
71121042 |
X |
+ |
26627737 |
HeLa |
viability after 12 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.4946166295357566 |
[289] |
[370,234,418] |
8 |
hSpCas9 |
negative selection |
1587218 |
71121386 |
71121409 |
X |
- |
26627737 |
HeLa |
viability after 12 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
0.44463073440017975 |
[406] |
[221,233,229] |
4 |
hSpCas9 |
negative selection |
1587219 |
71121596 |
71121619 |
X |
- |
26627737 |
HeLa |
viability after 12 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-1.5162076507100946 |
[404] |
[24,44,105] |
-8 |
hSpCas9 |
negative selection |
1587220 |
71118815 |
71118838 |
X |
- |
26627737 |
HeLa |
viability after 15 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.15844486011820846 |
[148] |
[55,52,53] |
-1 |
hSpCas9 |
negative selection |
1669530 |
71119735 |
71119758 |
X |
- |
26627737 |
HeLa |
viability after 15 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
0.38081723644265697 |
[1156] |
[537,506,810] |
3 |
hSpCas9 |
negative selection |
1669531 |
71120087 |
71120110 |
X |
- |
26627737 |
HeLa |
viability after 15 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.8931688170655586 |
[149] |
[105,124,108] |
6 |
hSpCas9 |
negative selection |
1669532 |
71121019 |
71121042 |
X |
+ |
26627737 |
HeLa |
viability after 15 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.0773637228611173 |
[289] |
[282,189,275] |
7 |
hSpCas9 |
negative selection |
1669533 |
71121386 |
71121409 |
X |
- |
26627737 |
HeLa |
viability after 15 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-0.24231324453559475 |
[406] |
[106,120,196] |
-2 |
hSpCas9 |
negative selection |
1669534 |
71121596 |
71121619 |
X |
- |
26627737 |
HeLa |
viability after 15 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-0.6009094986755663 |
[404] |
[41,151,134] |
-5 |
hSpCas9 |
negative selection |
1669535 |
71118815 |
71118838 |
X |
- |
26627737 |
HeLa |
viability after 18 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.09546141204365743 |
[148] |
[38,47,53] |
-1 |
hSpCas9 |
negative selection |
1751845 |
71119735 |
71119758 |
X |
- |
26627737 |
HeLa |
viability after 18 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
0.37131966232918456 |
[1156] |
[360,409,810] |
3 |
hSpCas9 |
negative selection |
1751846 |
71120087 |
71120110 |
X |
- |
26627737 |
HeLa |
viability after 18 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.8818427439736802 |
[149] |
[72,98,108] |
6 |
hSpCas9 |
negative selection |
1751847 |
71121019 |
71121042 |
X |
+ |
26627737 |
HeLa |
viability after 18 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.1226605719145621 |
[289] |
[207,153,275] |
7 |
hSpCas9 |
negative selection |
1751848 |
71121386 |
71121409 |
X |
- |
26627737 |
HeLa |
viability after 18 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-0.2388566593557968 |
[406] |
[66,106,196] |
-2 |
hSpCas9 |
negative selection |
1751849 |
71121596 |
71121619 |
X |
- |
26627737 |
HeLa |
viability after 18 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-0.5609984412885951 |
[404] |
[29,130,134] |
-5 |
hSpCas9 |
negative selection |
1751850 |
71118815 |
71118838 |
X |
- |
26627737 |
HCT116 |
viability after 6 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
1.041276442697969 |
[235] |
[212,0] |
5 |
hSpCas9 |
negative selection |
1834160 |
71119735 |
71119758 |
X |
- |
26627737 |
HCT116 |
viability after 6 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-0.14066461472090108 |
[1176] |
[172,164] |
-1 |
hSpCas9 |
negative selection |
1834161 |
71120087 |
71120110 |
X |
- |
26627737 |
HCT116 |
viability after 6 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.4982392688323243 |
[258] |
[52,59] |
2 |
hSpCas9 |
negative selection |
1834162 |
71121019 |
71121042 |
X |
+ |
26627737 |
HCT116 |
viability after 6 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.1329645586585722 |
[413] |
[134,146] |
6 |
hSpCas9 |
negative selection |
1834163 |
71121386 |
71121409 |
X |
- |
26627737 |
HCT116 |
viability after 6 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
0.2822349516900573 |
[963] |
[153,200] |
1 |
hSpCas9 |
negative selection |
1834164 |
71121596 |
71121619 |
X |
- |
26627737 |
HCT116 |
viability after 6 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
2.5707178564546505 |
[260] |
[32,359] |
9 |
hSpCas9 |
negative selection |
1834165 |
71118815 |
71118838 |
X |
- |
26627737 |
HCT116 |
viability after 8 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.1682756395591738 |
[104] |
[63,64,25] |
-2 |
hSpCas9 |
negative selection |
1916475 |
71119735 |
71119758 |
X |
- |
26627737 |
HCT116 |
viability after 8 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-0.1452198339324321 |
[653] |
[313,388,274] |
-2 |
hSpCas9 |
negative selection |
1916476 |
71120087 |
71120110 |
X |
- |
26627737 |
HCT116 |
viability after 8 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.26595023783881616 |
[192] |
[154,91,136] |
3 |
hSpCas9 |
negative selection |
1916477 |
71121019 |
71121042 |
X |
+ |
26627737 |
HCT116 |
viability after 8 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
-0.2384825737496481 |
[500] |
[188,178,331] |
-3 |
hSpCas9 |
negative selection |
1916478 |
71121386 |
71121409 |
X |
- |
26627737 |
HCT116 |
viability after 8 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-0.8201885633327237 |
[448] |
[142,101,174] |
-7 |
hSpCas9 |
negative selection |
1916479 |
71121596 |
71121619 |
X |
- |
26627737 |
HCT116 |
viability after 8 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-0.46658240276869867 |
[103] |
[53,58,11] |
-5 |
hSpCas9 |
negative selection |
1916480 |
71118815 |
71118838 |
X |
- |
26627737 |
HCT116 |
viability after 9 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-1.178677981566742 |
[235] |
[57,3] |
-7 |
hSpCas9 |
negative selection |
1998790 |
71119735 |
71119758 |
X |
- |
26627737 |
HCT116 |
viability after 9 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
0.002184744120894533 |
[1176] |
[235,376] |
0 |
hSpCas9 |
negative selection |
1998791 |
71120087 |
71120110 |
X |
- |
26627737 |
HCT116 |
viability after 9 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.638277258280352 |
[258] |
[43,4] |
-8 |
hSpCas9 |
negative selection |
1998792 |
71121019 |
71121042 |
X |
+ |
26627737 |
HCT116 |
viability after 9 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.5058752262209442 |
[413] |
[99,201] |
4 |
hSpCas9 |
negative selection |
1998793 |
71121386 |
71121409 |
X |
- |
26627737 |
HCT116 |
viability after 9 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-2.679487396418932 |
[963] |
[47,33] |
-9 |
hSpCas9 |
negative selection |
1998794 |
71121596 |
71121619 |
X |
- |
26627737 |
HCT116 |
viability after 9 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-0.4385624320907584 |
[260] |
[75,31] |
-3 |
hSpCas9 |
negative selection |
1998795 |
71118815 |
71118838 |
X |
- |
26627737 |
HCT116 |
viability after 12 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.13882384284865723 |
[104] |
[28,123,0] |
-1 |
hSpCas9 |
negative selection |
2081105 |
71119735 |
71119758 |
X |
- |
26627737 |
HCT116 |
viability after 12 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-0.6579460574816363 |
[653] |
[173,162,318] |
-6 |
hSpCas9 |
negative selection |
2081106 |
71120087 |
71120110 |
X |
- |
26627737 |
HCT116 |
viability after 12 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.33392578135939355 |
[192] |
[47,110,85] |
-4 |
hSpCas9 |
negative selection |
2081107 |
71121019 |
71121042 |
X |
+ |
26627737 |
HCT116 |
viability after 12 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
-0.38382745422200165 |
[500] |
[163,173,269] |
-4 |
hSpCas9 |
negative selection |
2081108 |
71121386 |
71121409 |
X |
- |
26627737 |
HCT116 |
viability after 12 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-0.9468463101595623 |
[448] |
[120,107,137] |
-8 |
hSpCas9 |
negative selection |
2081109 |
71121596 |
71121619 |
X |
- |
26627737 |
HCT116 |
viability after 12 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-0.28139076652635064 |
[103] |
[11,52,72] |
-3 |
hSpCas9 |
negative selection |
2081110 |
71118815 |
71118838 |
X |
- |
26627737 |
HCT116 |
viability after 15 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.18418925301722733 |
[104] |
[119,46,0] |
-2 |
hSpCas9 |
negative selection |
2163420 |
71119735 |
71119758 |
X |
- |
26627737 |
HCT116 |
viability after 15 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-0.7935595652700849 |
[653] |
[129,333,175] |
-7 |
hSpCas9 |
negative selection |
2163421 |
71120087 |
71120110 |
X |
- |
26627737 |
HCT116 |
viability after 15 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.3586191543447449 |
[192] |
[101,53,104] |
-4 |
hSpCas9 |
negative selection |
2163422 |
71121019 |
71121042 |
X |
+ |
26627737 |
HCT116 |
viability after 15 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
-0.08413306636277029 |
[500] |
[372,129,322] |
-1 |
hSpCas9 |
negative selection |
2163423 |
71121386 |
71121409 |
X |
- |
26627737 |
HCT116 |
viability after 15 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-1.2240633140005648 |
[448] |
[49,96,175] |
-8 |
hSpCas9 |
negative selection |
2163424 |
71121596 |
71121619 |
X |
- |
26627737 |
HCT116 |
viability after 15 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-1.1498163091439944 |
[103] |
[50,31,0] |
-8 |
hSpCas9 |
negative selection |
2163425 |
71118815 |
71118838 |
X |
- |
26627737 |
HCT116 |
viability after 18 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-0.7652302400017443 |
[104] |
[17,56,11] |
-6 |
hSpCas9 |
negative selection |
2245735 |
71119735 |
71119758 |
X |
- |
26627737 |
HCT116 |
viability after 18 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-1.0042536194423737 |
[653] |
[60,238,167] |
-7 |
hSpCas9 |
negative selection |
2245736 |
71120087 |
71120110 |
X |
- |
26627737 |
HCT116 |
viability after 18 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.2858524569560841 |
[192] |
[54,81,92] |
-3 |
hSpCas9 |
negative selection |
2245737 |
71121019 |
71121042 |
X |
+ |
26627737 |
HCT116 |
viability after 18 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.054631668914201015 |
[500] |
[401,49,318] |
0 |
hSpCas9 |
negative selection |
2245738 |
71121386 |
71121409 |
X |
- |
26627737 |
HCT116 |
viability after 18 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-1.572669331241535 |
[448] |
[66,31,124] |
-8 |
hSpCas9 |
negative selection |
2245739 |
71121596 |
71121619 |
X |
- |
26627737 |
HCT116 |
viability after 18 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-1.3467002944082456 |
[103] |
[33,7,17] |
-8 |
hSpCas9 |
negative selection |
2245740 |
71118746 |
71118769 |
X |
+ |
24336569 |
HL60 |
viability |
CTGGGCAAGATGGCGGCCTTCGG |
MED12 |
ENSG00000184634 |
1.2655705701542057 |
[318] |
[1622] |
8 |
hSpCas9 |
negative selection |
2276833 |
71118762 |
71118785 |
X |
- |
24336569 |
HL60 |
viability |
TTCGTAGCTCAAGATCCCGAAGG |
MED12 |
ENSG00000184634 |
-0.7576431189085765 |
[913] |
[1143] |
-6 |
hSpCas9 |
negative selection |
2276834 |
71118768 |
71118791 |
X |
+ |
24336569 |
HL60 |
viability |
GGATCTTGAGCTACGAACACCGG |
MED12 |
ENSG00000184634 |
-0.29153324351521426 |
[951] |
[1645] |
-3 |
hSpCas9 |
negative selection |
2276835 |
71118814 |
71118837 |
X |
+ |
24336569 |
HL60 |
viability |
GCCTCCCGATGTTTACCCTCAGG |
MED12 |
ENSG00000184634 |
-0.47974308164637347 |
[484] |
[735] |
-4 |
hSpCas9 |
negative selection |
2276836 |
71118839 |
71118862 |
X |
- |
24336569 |
HL60 |
viability |
GAACGCACCTCCTTCTGTTTGGG |
MED12 |
ENSG00000184634 |
1.0875120714198672 |
[337] |
[1519] |
8 |
hSpCas9 |
negative selection |
2276837 |
71119363 |
71119386 |
X |
+ |
24336569 |
HL60 |
viability |
CCTGCCTCAGGATGAACTGACGG |
MED12 |
ENSG00000184634 |
-1.5141146127018335 |
[466] |
[345] |
-8 |
hSpCas9 |
negative selection |
2276838 |
71119409 |
71119432 |
X |
+ |
24336569 |
HL60 |
viability |
AATAACCAGCCTGCTGTCTCTGG |
MED12 |
ENSG00000184634 |
0.5901783532047609 |
[252] |
[805] |
5 |
hSpCas9 |
negative selection |
2276839 |
71119449 |
71119472 |
X |
- |
24336569 |
HL60 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.7005275940096107 |
[1005] |
[1309] |
-6 |
hSpCas9 |
negative selection |
2276840 |
71119456 |
71119479 |
X |
+ |
24336569 |
HL60 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.03386935548978365 |
[804] |
[1663] |
0 |
hSpCas9 |
negative selection |
2276841 |
71119469 |
71119492 |
X |
- |
24336569 |
HL60 |
viability |
CAGAGTTGTCTCACCTTGGCAGG |
MED12 |
ENSG00000184634 |
-0.1839377218786893 |
[473] |
[882] |
-1 |
hSpCas9 |
negative selection |
2276842 |
71118746 |
71118769 |
X |
+ |
24336569 |
KBM7 |
viability |
CTGGGCAAGATGGCGGCCTTCGG |
MED12 |
ENSG00000184634 |
1.0044941655472515 |
[410] |
[2248] |
8 |
hSpCas9 |
negative selection |
2344010 |
71118762 |
71118785 |
X |
- |
24336569 |
KBM7 |
viability |
TTCGTAGCTCAAGATCCCGAAGG |
MED12 |
ENSG00000184634 |
-0.6621342274094444 |
[871] |
[1502] |
-5 |
hSpCas9 |
negative selection |
2344011 |
71118768 |
71118791 |
X |
+ |
24336569 |
KBM7 |
viability |
GGATCTTGAGCTACGAACACCGG |
MED12 |
ENSG00000184634 |
-3.097174903624821 |
[912] |
[290] |
-9 |
hSpCas9 |
negative selection |
2344012 |
71118814 |
71118837 |
X |
+ |
24336569 |
KBM7 |
viability |
GCCTCCCGATGTTTACCCTCAGG |
MED12 |
ENSG00000184634 |
-1.1872388998843522 |
[267] |
[320] |
-7 |
hSpCas9 |
negative selection |
2344013 |
71118839 |
71118862 |
X |
- |
24336569 |
KBM7 |
viability |
GAACGCACCTCCTTCTGTTTGGG |
MED12 |
ENSG00000184634 |
0.9425949156783586 |
[416] |
[2185] |
7 |
hSpCas9 |
negative selection |
2344014 |
71119363 |
71119386 |
X |
+ |
24336569 |
KBM7 |
viability |
CCTGCCTCAGGATGAACTGACGG |
MED12 |
ENSG00000184634 |
-0.3030976904363754 |
[374] |
[828] |
-3 |
hSpCas9 |
negative selection |
2344015 |
71119409 |
71119432 |
X |
+ |
24336569 |
KBM7 |
viability |
AATAACCAGCCTGCTGTCTCTGG |
MED12 |
ENSG00000184634 |
-0.4917017497811902 |
[165] |
[321] |
-4 |
hSpCas9 |
negative selection |
2344016 |
71119449 |
71119472 |
X |
- |
24336569 |
KBM7 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.35521103357691475 |
[813] |
[2839] |
3 |
hSpCas9 |
negative selection |
2344017 |
71119456 |
71119479 |
X |
+ |
24336569 |
KBM7 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.748077613289155 |
[709] |
[1152] |
-5 |
hSpCas9 |
negative selection |
2344018 |
71119469 |
71119492 |
X |
- |
24336569 |
KBM7 |
viability |
CAGAGTTGTCTCACCTTGGCAGG |
MED12 |
ENSG00000184634 |
0.17235944241524837 |
[162] |
[500] |
1 |
hSpCas9 |
negative selection |
2344019 |
71133998 |
71134021 |
X |
+ |
25494202 |
A375 |
resistance to PLX-4720 (puromycin) |
GGTGGGCGGATCACGAGGTCAGG |
MED12 |
ENSG00000184634 |
2.37985785728498 |
[230,76] |
[300,38] |
7 |
dCas9-VP64 |
positive selection |
2475743 |
71133998 |
71134021 |
X |
+ |
25494202 |
A375 |
resistance to PLX-4720 (zeocin) |
GGTGGGCGGATCACGAGGTCAGG |
MED12 |
ENSG00000184634 |
0.17249846111827716 |
[159,84] |
[44,44] |
1 |
dCas9-VP64 |
positive selection |
2570998 |
71118814 |
71118837 |
X |
+ |
27260157 |
DLD1 |
viability |
GCCTCCCGATGTTTACCCTCAGG |
MED12 |
ENSG00000184634 |
-2.04555915456445 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2574133 |
71121107 |
71121130 |
X |
- |
27260157 |
DLD1 |
viability |
TCTCGGTGTAATCCCACTGCCGG |
MED12 |
ENSG00000184634 |
-2.50130598915307 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2578732 |
71119363 |
71119386 |
X |
+ |
27260157 |
DLD1 |
viability |
CCTGCCTCAGGATGAACTGACGG |
MED12 |
ENSG00000184634 |
-1.9190349277028 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2578826 |
71121018 |
71121041 |
X |
+ |
27260157 |
DLD1 |
viability |
ATGGCTGAATACTACCGGCCAGG |
MED12 |
ENSG00000184634 |
0.260560893107487 |
[] |
[] |
4 |
hSpCas9 |
negative selection |
2586068 |
71119456 |
71119479 |
X |
+ |
27260157 |
DLD1 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-1.87480949173598 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2586237 |
71119849 |
71119872 |
X |
- |
27260157 |
DLD1 |
viability |
GGCTAGTTGCGTGAGTGGCTTGG |
MED12 |
ENSG00000184634 |
-2.96039065120315 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2604412 |
71118762 |
71118785 |
X |
- |
27260157 |
DLD1 |
viability |
TTCGTAGCTCAAGATCCCGAAGG |
MED12 |
ENSG00000184634 |
-3.1830070629913 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2604881 |
71119807 |
71119830 |
X |
+ |
27260157 |
DLD1 |
viability |
CCCAGAGTGCCATTAACACTTGG |
MED12 |
ENSG00000184634 |
-1.07530422431088 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2606545 |
71120087 |
71120110 |
X |
- |
27260157 |
DLD1 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.878985967852321 |
[] |
[] |
-6 |
hSpCas9 |
negative selection |
2606774 |
71118839 |
71118862 |
X |
- |
27260157 |
DLD1 |
viability |
GAACGCACCTCCTTCTGTTTGGG |
MED12 |
ENSG00000184634 |
-0.92701316920734 |
[] |
[] |
-6 |
hSpCas9 |
negative selection |
2607596 |
71119409 |
71119432 |
X |
+ |
27260157 |
DLD1 |
viability |
AATAACCAGCCTGCTGTCTCTGG |
MED12 |
ENSG00000184634 |
-1.05206306270786 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2611813 |
71120105 |
71120128 |
X |
- |
27260157 |
DLD1 |
viability |
GATTGCTGCATAGTAGGCACAGG |
MED12 |
ENSG00000184634 |
-1.22624656087264 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2614563 |
71119469 |
71119492 |
X |
- |
27260157 |
DLD1 |
viability |
CAGAGTTGTCTCACCTTGGCAGG |
MED12 |
ENSG00000184634 |
-3.18146407172987 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2615890 |
71118768 |
71118791 |
X |
+ |
27260157 |
DLD1 |
viability |
GGATCTTGAGCTACGAACACCGG |
MED12 |
ENSG00000184634 |
-2.79527216435593 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2618078 |
71120071 |
71120094 |
X |
- |
27260157 |
DLD1 |
viability |
AGCCAGGCAGCCCGCATCACAGG |
MED12 |
ENSG00000184634 |
-2.93592694100047 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2622683 |
71119735 |
71119758 |
X |
- |
27260157 |
DLD1 |
viability |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.22504544364054 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2624218 |
71118746 |
71118769 |
X |
+ |
27260157 |
DLD1 |
viability |
CTGGGCAAGATGGCGGCCTTCGG |
MED12 |
ENSG00000184634 |
1.31444750301894 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
2642727 |
71118733 |
71118756 |
X |
- |
27260157 |
DLD1 |
viability |
TCTTGCCCAGCCCGTAGCGCCGG |
MED12 |
ENSG00000184634 |
-1.04656977425945 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2645947 |
71119449 |
71119472 |
X |
- |
27260157 |
DLD1 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-1.54300067978329 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2646707 |
71119807 |
71119830 |
X |
- |
27260157 |
DLD1 |
viability |
CCAAGTGTTAATGGCACTCTGGG |
MED12 |
ENSG00000184634 |
-0.603761142849326 |
[] |
[] |
-5 |
hSpCas9 |
negative selection |
2647566 |
71118814 |
71118837 |
X |
+ |
27260157 |
HT1080 |
viability |
GCCTCCCGATGTTTACCCTCAGG |
MED12 |
ENSG00000184634 |
-0.848598076680517 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2650263 |
71121107 |
71121130 |
X |
- |
27260157 |
HT1080 |
viability |
TCTCGGTGTAATCCCACTGCCGG |
MED12 |
ENSG00000184634 |
-2.38029754015734 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2654862 |
71119363 |
71119386 |
X |
+ |
27260157 |
HT1080 |
viability |
CCTGCCTCAGGATGAACTGACGG |
MED12 |
ENSG00000184634 |
-1.12517709062541 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2654956 |
71121018 |
71121041 |
X |
+ |
27260157 |
HT1080 |
viability |
ATGGCTGAATACTACCGGCCAGG |
MED12 |
ENSG00000184634 |
-0.0522509830959634 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2662198 |
71119456 |
71119479 |
X |
+ |
27260157 |
HT1080 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.550697138657013 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2662367 |
71119849 |
71119872 |
X |
- |
27260157 |
HT1080 |
viability |
GGCTAGTTGCGTGAGTGGCTTGG |
MED12 |
ENSG00000184634 |
-0.0842050702807577 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2680542 |
71118762 |
71118785 |
X |
- |
27260157 |
HT1080 |
viability |
TTCGTAGCTCAAGATCCCGAAGG |
MED12 |
ENSG00000184634 |
-0.382472308113742 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2681011 |
71119807 |
71119830 |
X |
+ |
27260157 |
HT1080 |
viability |
CCCAGAGTGCCATTAACACTTGG |
MED12 |
ENSG00000184634 |
0.152907110414912 |
[] |
[] |
1 |
hSpCas9 |
negative selection |
2682675 |
71120087 |
71120110 |
X |
- |
27260157 |
HT1080 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.358185261643419 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2682904 |
71118839 |
71118862 |
X |
- |
27260157 |
HT1080 |
viability |
GAACGCACCTCCTTCTGTTTGGG |
MED12 |
ENSG00000184634 |
-0.510586803298333 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2683726 |
71119409 |
71119432 |
X |
+ |
27260157 |
HT1080 |
viability |
AATAACCAGCCTGCTGTCTCTGG |
MED12 |
ENSG00000184634 |
-0.913633800618034 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2687943 |
71120105 |
71120128 |
X |
- |
27260157 |
HT1080 |
viability |
GATTGCTGCATAGTAGGCACAGG |
MED12 |
ENSG00000184634 |
-0.936820445116831 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2690693 |
71119469 |
71119492 |
X |
- |
27260157 |
HT1080 |
viability |
CAGAGTTGTCTCACCTTGGCAGG |
MED12 |
ENSG00000184634 |
-0.0497911537849418 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2692020 |
71118768 |
71118791 |
X |
+ |
27260157 |
HT1080 |
viability |
GGATCTTGAGCTACGAACACCGG |
MED12 |
ENSG00000184634 |
-0.843150738196219 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2694208 |
71120071 |
71120094 |
X |
- |
27260157 |
HT1080 |
viability |
AGCCAGGCAGCCCGCATCACAGG |
MED12 |
ENSG00000184634 |
-0.311282631164269 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2698813 |
71119735 |
71119758 |
X |
- |
27260157 |
HT1080 |
viability |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-0.192593122281293 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2700348 |
71118746 |
71118769 |
X |
+ |
27260157 |
HT1080 |
viability |
CTGGGCAAGATGGCGGCCTTCGG |
MED12 |
ENSG00000184634 |
1.68211478253099 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
2718857 |
71118733 |
71118756 |
X |
- |
27260157 |
HT1080 |
viability |
TCTTGCCCAGCCCGTAGCGCCGG |
MED12 |
ENSG00000184634 |
-0.187590911658117 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2722077 |
71119449 |
71119472 |
X |
- |
27260157 |
HT1080 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
1.70402344757441 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
2722837 |
71119807 |
71119830 |
X |
- |
27260157 |
HT1080 |
viability |
CCAAGTGTTAATGGCACTCTGGG |
MED12 |
ENSG00000184634 |
-1.75634278254259 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2723696 |
71118814 |
71118837 |
X |
+ |
27260157 |
MKN45 |
viability |
GCCTCCCGATGTTTACCCTCAGG |
MED12 |
ENSG00000184634 |
-2.04135885423869 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2726393 |
71121107 |
71121130 |
X |
- |
27260157 |
MKN45 |
viability |
TCTCGGTGTAATCCCACTGCCGG |
MED12 |
ENSG00000184634 |
-2.18998197756133 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2730992 |
71119363 |
71119386 |
X |
+ |
27260157 |
MKN45 |
viability |
CCTGCCTCAGGATGAACTGACGG |
MED12 |
ENSG00000184634 |
-1.62958492619198 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2731086 |
71121018 |
71121041 |
X |
+ |
27260157 |
MKN45 |
viability |
ATGGCTGAATACTACCGGCCAGG |
MED12 |
ENSG00000184634 |
1.14320145808125 |
[] |
[] |
8 |
hSpCas9 |
negative selection |
2738328 |
71119456 |
71119479 |
X |
+ |
27260157 |
MKN45 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-1.09195208625038 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2738497 |
71119849 |
71119872 |
X |
- |
27260157 |
MKN45 |
viability |
GGCTAGTTGCGTGAGTGGCTTGG |
MED12 |
ENSG00000184634 |
-1.14637296557975 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2756672 |
71118762 |
71118785 |
X |
- |
27260157 |
MKN45 |
viability |
TTCGTAGCTCAAGATCCCGAAGG |
MED12 |
ENSG00000184634 |
-0.711917492305867 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2757141 |
71119807 |
71119830 |
X |
+ |
27260157 |
MKN45 |
viability |
CCCAGAGTGCCATTAACACTTGG |
MED12 |
ENSG00000184634 |
-1.14560843259963 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2758805 |
71120087 |
71120110 |
X |
- |
27260157 |
MKN45 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.267872601036431 |
[] |
[] |
-1 |
hSpCas9 |
negative selection |
2759034 |
71118839 |
71118862 |
X |
- |
27260157 |
MKN45 |
viability |
GAACGCACCTCCTTCTGTTTGGG |
MED12 |
ENSG00000184634 |
-0.0193854645415899 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2759856 |
71119409 |
71119432 |
X |
+ |
27260157 |
MKN45 |
viability |
AATAACCAGCCTGCTGTCTCTGG |
MED12 |
ENSG00000184634 |
-0.561473051578904 |
[] |
[] |
-6 |
hSpCas9 |
negative selection |
2764073 |
71120105 |
71120128 |
X |
- |
27260157 |
MKN45 |
viability |
GATTGCTGCATAGTAGGCACAGG |
MED12 |
ENSG00000184634 |
-1.1306889279307 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2766823 |
71119469 |
71119492 |
X |
- |
27260157 |
MKN45 |
viability |
CAGAGTTGTCTCACCTTGGCAGG |
MED12 |
ENSG00000184634 |
-0.108775840570309 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2768150 |
71118768 |
71118791 |
X |
+ |
27260157 |
MKN45 |
viability |
GGATCTTGAGCTACGAACACCGG |
MED12 |
ENSG00000184634 |
-1.51188982617536 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2770338 |
71120071 |
71120094 |
X |
- |
27260157 |
MKN45 |
viability |
AGCCAGGCAGCCCGCATCACAGG |
MED12 |
ENSG00000184634 |
-1.84252695466703 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2774943 |
71119735 |
71119758 |
X |
- |
27260157 |
MKN45 |
viability |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-1.01045848827736 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2776478 |
71118746 |
71118769 |
X |
+ |
27260157 |
MKN45 |
viability |
CTGGGCAAGATGGCGGCCTTCGG |
MED12 |
ENSG00000184634 |
1.58689540788805 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
2794987 |
71118733 |
71118756 |
X |
- |
27260157 |
MKN45 |
viability |
TCTTGCCCAGCCCGTAGCGCCGG |
MED12 |
ENSG00000184634 |
-1.73786740589868 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2798207 |
71119449 |
71119472 |
X |
- |
27260157 |
MKN45 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.223248374821521 |
[] |
[] |
-1 |
hSpCas9 |
negative selection |
2798967 |
71119807 |
71119830 |
X |
- |
27260157 |
MKN45 |
viability |
CCAAGTGTTAATGGCACTCTGGG |
MED12 |
ENSG00000184634 |
-2.44741896972472 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2799826 |
71118814 |
71118837 |
X |
+ |
27260157 |
RKO |
viability |
GCCTCCCGATGTTTACCCTCAGG |
MED12 |
ENSG00000184634 |
-1.44024266038694 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2802523 |
71121107 |
71121130 |
X |
- |
27260157 |
RKO |
viability |
TCTCGGTGTAATCCCACTGCCGG |
MED12 |
ENSG00000184634 |
-2.26137710189155 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2807122 |
71119363 |
71119386 |
X |
+ |
27260157 |
RKO |
viability |
CCTGCCTCAGGATGAACTGACGG |
MED12 |
ENSG00000184634 |
-1.38313855329316 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2807216 |
71121018 |
71121041 |
X |
+ |
27260157 |
RKO |
viability |
ATGGCTGAATACTACCGGCCAGG |
MED12 |
ENSG00000184634 |
0.120556433562351 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2814458 |
71119456 |
71119479 |
X |
+ |
27260157 |
RKO |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.142809600952273 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2814627 |
71119849 |
71119872 |
X |
- |
27260157 |
RKO |
viability |
GGCTAGTTGCGTGAGTGGCTTGG |
MED12 |
ENSG00000184634 |
-2.31604111850443 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2832802 |
71118762 |
71118785 |
X |
- |
27260157 |
RKO |
viability |
TTCGTAGCTCAAGATCCCGAAGG |
MED12 |
ENSG00000184634 |
0.0178519843012622 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2833271 |
71119807 |
71119830 |
X |
+ |
27260157 |
RKO |
viability |
CCCAGAGTGCCATTAACACTTGG |
MED12 |
ENSG00000184634 |
-1.04605003421434 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2834935 |
71120087 |
71120110 |
X |
- |
27260157 |
RKO |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.12314408052973 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2835164 |
71118839 |
71118862 |
X |
- |
27260157 |
RKO |
viability |
GAACGCACCTCCTTCTGTTTGGG |
MED12 |
ENSG00000184634 |
-0.599136689878281 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2835986 |
71119409 |
71119432 |
X |
+ |
27260157 |
RKO |
viability |
AATAACCAGCCTGCTGTCTCTGG |
MED12 |
ENSG00000184634 |
0.140195582441406 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2840203 |
71120105 |
71120128 |
X |
- |
27260157 |
RKO |
viability |
GATTGCTGCATAGTAGGCACAGG |
MED12 |
ENSG00000184634 |
-1.78376116293228 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2842953 |
71119469 |
71119492 |
X |
- |
27260157 |
RKO |
viability |
CAGAGTTGTCTCACCTTGGCAGG |
MED12 |
ENSG00000184634 |
0.14395461536466 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2844280 |
71118768 |
71118791 |
X |
+ |
27260157 |
RKO |
viability |
GGATCTTGAGCTACGAACACCGG |
MED12 |
ENSG00000184634 |
-2.00289063670625 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2846468 |
71120071 |
71120094 |
X |
- |
27260157 |
RKO |
viability |
AGCCAGGCAGCCCGCATCACAGG |
MED12 |
ENSG00000184634 |
-1.52567811286189 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2851073 |
71119735 |
71119758 |
X |
- |
27260157 |
RKO |
viability |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-1.7543141987663 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2852608 |
71118746 |
71118769 |
X |
+ |
27260157 |
RKO |
viability |
CTGGGCAAGATGGCGGCCTTCGG |
MED12 |
ENSG00000184634 |
1.02209861506741 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
2871117 |
71118733 |
71118756 |
X |
- |
27260157 |
RKO |
viability |
TCTTGCCCAGCCCGTAGCGCCGG |
MED12 |
ENSG00000184634 |
-0.663250334874068 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2874337 |
71119449 |
71119472 |
X |
- |
27260157 |
RKO |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.449477865226897 |
[] |
[] |
2 |
hSpCas9 |
negative selection |
2875097 |
71119807 |
71119830 |
X |
- |
27260157 |
RKO |
viability |
CCAAGTGTTAATGGCACTCTGGG |
MED12 |
ENSG00000184634 |
-1.92569955410822 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
2875956 |
71118814 |
71118837 |
X |
+ |
27260157 |
SF268 |
viability |
GCCTCCCGATGTTTACCCTCAGG |
MED12 |
ENSG00000184634 |
-0.341184976102244 |
[] |
[] |
-3 |
hSpCas9 |
negative selection |
2878653 |
71121107 |
71121130 |
X |
- |
27260157 |
SF268 |
viability |
TCTCGGTGTAATCCCACTGCCGG |
MED12 |
ENSG00000184634 |
-1.0879546250063 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2883252 |
71119363 |
71119386 |
X |
+ |
27260157 |
SF268 |
viability |
CCTGCCTCAGGATGAACTGACGG |
MED12 |
ENSG00000184634 |
-0.165773043515729 |
[] |
[] |
-1 |
hSpCas9 |
negative selection |
2883346 |
71121018 |
71121041 |
X |
+ |
27260157 |
SF268 |
viability |
ATGGCTGAATACTACCGGCCAGG |
MED12 |
ENSG00000184634 |
0.626448873565086 |
[] |
[] |
8 |
hSpCas9 |
negative selection |
2890588 |
71119456 |
71119479 |
X |
+ |
27260157 |
SF268 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.102958868271169 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2890757 |
71119849 |
71119872 |
X |
- |
27260157 |
SF268 |
viability |
GGCTAGTTGCGTGAGTGGCTTGG |
MED12 |
ENSG00000184634 |
-0.381804288286813 |
[] |
[] |
-3 |
hSpCas9 |
negative selection |
2908932 |
71118762 |
71118785 |
X |
- |
27260157 |
SF268 |
viability |
TTCGTAGCTCAAGATCCCGAAGG |
MED12 |
ENSG00000184634 |
-0.274025227983948 |
[] |
[] |
-2 |
hSpCas9 |
negative selection |
2909401 |
71119807 |
71119830 |
X |
+ |
27260157 |
SF268 |
viability |
CCCAGAGTGCCATTAACACTTGG |
MED12 |
ENSG00000184634 |
0.362637707982303 |
[] |
[] |
4 |
hSpCas9 |
negative selection |
2911065 |
71120087 |
71120110 |
X |
- |
27260157 |
SF268 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.713426682336917 |
[] |
[] |
-5 |
hSpCas9 |
negative selection |
2911294 |
71118839 |
71118862 |
X |
- |
27260157 |
SF268 |
viability |
GAACGCACCTCCTTCTGTTTGGG |
MED12 |
ENSG00000184634 |
0.112459664243668 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2912116 |
71119409 |
71119432 |
X |
+ |
27260157 |
SF268 |
viability |
AATAACCAGCCTGCTGTCTCTGG |
MED12 |
ENSG00000184634 |
-0.705157308860554 |
[] |
[] |
-5 |
hSpCas9 |
negative selection |
2916333 |
71120105 |
71120128 |
X |
- |
27260157 |
SF268 |
viability |
GATTGCTGCATAGTAGGCACAGG |
MED12 |
ENSG00000184634 |
-1.57962867116393 |
[] |
[] |
-8 |
hSpCas9 |
negative selection |
2919083 |
71119469 |
71119492 |
X |
- |
27260157 |
SF268 |
viability |
CAGAGTTGTCTCACCTTGGCAGG |
MED12 |
ENSG00000184634 |
-0.385743217077167 |
[] |
[] |
-3 |
hSpCas9 |
negative selection |
2920410 |
71118768 |
71118791 |
X |
+ |
27260157 |
SF268 |
viability |
GGATCTTGAGCTACGAACACCGG |
MED12 |
ENSG00000184634 |
0.468019325977523 |
[] |
[] |
7 |
hSpCas9 |
negative selection |
2922598 |
71120071 |
71120094 |
X |
- |
27260157 |
SF268 |
viability |
AGCCAGGCAGCCCGCATCACAGG |
MED12 |
ENSG00000184634 |
0.165472624790402 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2927203 |
71119735 |
71119758 |
X |
- |
27260157 |
SF268 |
viability |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-0.0488743800491198 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2928738 |
71118746 |
71118769 |
X |
+ |
27260157 |
SF268 |
viability |
CTGGGCAAGATGGCGGCCTTCGG |
MED12 |
ENSG00000184634 |
1.12015014750464 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
2947247 |
71118733 |
71118756 |
X |
- |
27260157 |
SF268 |
viability |
TCTTGCCCAGCCCGTAGCGCCGG |
MED12 |
ENSG00000184634 |
-1.16443901102937 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
2950467 |
71119449 |
71119472 |
X |
- |
27260157 |
SF268 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.732140549855535 |
[] |
[] |
8 |
hSpCas9 |
negative selection |
2951227 |
71119807 |
71119830 |
X |
- |
27260157 |
SF268 |
viability |
CCAAGTGTTAATGGCACTCTGGG |
MED12 |
ENSG00000184634 |
0.173242914437615 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
2952086 |
71124259 |
71124282 |
X |
+ |
27453484 |
HT29 |
resistance to T3SS1-dependent cytotoxicity |
CTTGCACTCTCATCTCCCGAGGG |
MED12 |
ENSG00000184634 |
-1.0680672713401778 |
[3,3] |
[1,0] |
-9 |
hSpCas9 |
positive selection |
3001800 |
71123191 |
71123214 |
X |
+ |
27453484 |
HT29 |
resistance to T3SS1-dependent cytotoxicity |
GCTCCTGGAGAAGAGACAGGCGG |
MED12 |
ENSG00000184634 |
-0.9057678910491498 |
[1,1] |
[0,0] |
-8 |
hSpCas9 |
positive selection |
3001801 |
71127015 |
71127038 |
X |
- |
27453484 |
HT29 |
resistance to T3SS1-dependent cytotoxicity |
GTAGCTGCCCACCAGATCCGAGG |
MED12 |
ENSG00000184634 |
-0.3795163032119768 |
[1,2] |
[2,0] |
-5 |
hSpCas9 |
positive selection |
3001802 |
71122303 |
71122326 |
X |
+ |
27453484 |
HT29 |
resistance to T3SS1-dependent cytotoxicity |
TCCAACCTGCCCATGCCAGAGGG |
MED12 |
ENSG00000184634 |
-0.0359435425183533 |
[1,1] |
[2,0] |
0 |
hSpCas9 |
positive selection |
3001803 |
71124259 |
71124282 |
X |
+ |
27453484 |
HT29 |
resistance to T3SS2-dependent cytotoxicity |
CTTGCACTCTCATCTCCCGAGGG |
MED12 |
ENSG00000184634 |
-0.6812902780794255 |
[3,3] |
[0,1] |
-8 |
hSpCas9 |
positive selection |
3069658 |
71123191 |
71123214 |
X |
+ |
27453484 |
HT29 |
resistance to T3SS2-dependent cytotoxicity |
GCTCCTGGAGAAGAGACAGGCGG |
MED12 |
ENSG00000184634 |
-0.6831133623883653 |
[1,1] |
[0,0] |
-8 |
hSpCas9 |
positive selection |
3069659 |
71127015 |
71127038 |
X |
- |
27453484 |
HT29 |
resistance to T3SS2-dependent cytotoxicity |
GTAGCTGCCCACCAGATCCGAGG |
MED12 |
ENSG00000184634 |
-0.05062558529958894 |
[1,1] |
[2,0] |
0 |
hSpCas9 |
positive selection |
3069660 |
71122303 |
71122326 |
X |
+ |
27453484 |
HT29 |
resistance to T3SS2-dependent cytotoxicity |
TCCAACCTGCCCATGCCAGAGGG |
MED12 |
ENSG00000184634 |
0.23947837349424744 |
[1,1] |
[2,0] |
4 |
hSpCas9 |
positive selection |
3069661 |
71120087 |
71120110 |
|
- |
24336571 |
A375 |
resistance to PLX after 7 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
1.3669686061105661 |
[14,10] |
[32,34] |
9 |
hSpCas9 |
positive selection |
3126976 |
71119449 |
71119472 |
|
- |
24336571 |
A375 |
resistance to PLX after 7 days |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
1.4450735715186482 |
[14,15] |
[43,42] |
9 |
hSpCas9 |
positive selection |
3126977 |
71119456 |
71119479 |
|
+ |
24336571 |
A375 |
resistance to PLX after 7 days |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
2.1684751009431844 |
[18,16] |
[78,83] |
9 |
hSpCas9 |
positive selection |
3126978 |
71120111 |
71120134 |
|
- |
24336571 |
A375 |
resistance to PLX after 7 days |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
1.1488040807731987 |
[7,4] |
[16,13] |
9 |
hSpCas9 |
positive selection |
3126979 |
71120087 |
71120110 |
|
- |
24336571 |
A375 |
resistance to PLX after 14 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
7.354408622177448 |
[14,11] |
[1069,1071] |
9 |
hSpCas9 |
positive selection |
3184769 |
71119449 |
71119472 |
|
- |
24336571 |
A375 |
resistance to PLX after 14 days |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
7.814676432101597 |
[20,8] |
[1656,1663] |
9 |
hSpCas9 |
positive selection |
3184770 |
71119456 |
71119479 |
|
+ |
24336571 |
A375 |
resistance to PLX after 14 days |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
7.646374022672621 |
[28,19] |
[2271,2437] |
9 |
hSpCas9 |
positive selection |
3184771 |
71120111 |
71120134 |
|
- |
24336571 |
A375 |
resistance to PLX after 14 days |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
6.961411077847321 |
[5,5] |
[380,371] |
9 |
hSpCas9 |
positive selection |
3184772 |
71120087 |
71120110 |
|
- |
24336571 |
A375 |
viability after 7 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.13149157803261458 |
[11] |
[14,10] |
2 |
hSpCas9 |
negative selection |
3242562 |
71119449 |
71119472 |
|
- |
24336571 |
A375 |
viability after 7 days |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.6840759466221442 |
[9] |
[14,15] |
8 |
hSpCas9 |
negative selection |
3242563 |
71119456 |
71119479 |
|
+ |
24336571 |
A375 |
viability after 7 days |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.5639669211382554 |
[12] |
[18,16] |
8 |
hSpCas9 |
negative selection |
3242564 |
71120111 |
71120134 |
|
- |
24336571 |
A375 |
viability after 7 days |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
0.14041442221391187 |
[5] |
[7,4] |
2 |
hSpCas9 |
negative selection |
3242565 |
71120087 |
71120110 |
|
- |
24336571 |
A375 |
viability after 14 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.20519159397423475 |
[11] |
[14,11] |
2 |
hSpCas9 |
negative selection |
3300355 |
71119449 |
71119472 |
|
- |
24336571 |
A375 |
viability after 14 days |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.6581189561500427 |
[9] |
[20,8] |
8 |
hSpCas9 |
negative selection |
3300356 |
71119456 |
71119479 |
|
+ |
24336571 |
A375 |
viability after 14 days |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
1.0368928043908232 |
[12] |
[28,19] |
9 |
hSpCas9 |
negative selection |
3300357 |
71120111 |
71120134 |
|
- |
24336571 |
A375 |
viability after 14 days |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.007071531907917317 |
[5] |
[5,5] |
0 |
hSpCas9 |
negative selection |
3300358 |
71120111 |
71120134 |
X |
- |
27383988 |
293T |
resistance to West Nile virus (flavivirus) |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
0.5991147286940403 |
[100,100] |
[0,0] |
3 |
hSpCas9 |
positive selection |
3378903 |
71120087 |
71120110 |
X |
- |
27383988 |
293T |
resistance to West Nile virus (flavivirus) |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
1.7027373597681978 |
[46,46] |
[0,0] |
7 |
hSpCas9 |
positive selection |
3378904 |
71119456 |
71119479 |
X |
+ |
27383988 |
293T |
resistance to West Nile virus (flavivirus) |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.5628527509693527 |
[225,225] |
[0,0] |
-4 |
hSpCas9 |
positive selection |
3378905 |
71124258 |
71124281 |
X |
+ |
26780180 |
HT29 |
viability (Avana library 4 designs) |
CTTGCACTCTCATCTCCCGAGGG |
MED12 |
ENSG00000184634 |
5.07766209561948 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
3439528 |
71123190 |
71123213 |
X |
+ |
26780180 |
HT29 |
viability (Avana library 4 designs) |
GCTCCTGGAGAAGAGACAGGCGG |
MED12 |
ENSG00000184634 |
4.02707911857856 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
3439529 |
71127015 |
71127038 |
X |
- |
26780180 |
HT29 |
viability (Avana library 4 designs) |
GTAGCTGCCCACCAGATCCGAGG |
MED12 |
ENSG00000184634 |
3.62027293723238 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
3439530 |
71122302 |
71122325 |
X |
+ |
26780180 |
HT29 |
viability (Avana library 4 designs) |
TCCAACCTGCCCATGCCAGAGGG |
MED12 |
ENSG00000184634 |
3.10520671348402 |
[] |
[] |
8 |
hSpCas9 |
negative selection |
3439531 |
71123190 |
71123213 |
X |
+ |
26780180 |
A375 |
viability (Avana lentiCRISPRv2) |
GCTCCTGGAGAAGAGACAGGCGG |
MED12 |
ENSG00000184634 |
-8.53494434302362 |
[] |
[] |
-7 |
hSpCas9 |
negative selection |
3529315 |
71122302 |
71122325 |
X |
+ |
26780180 |
A375 |
viability (Avana lentiCRISPRv2) |
TCCAACCTGCCCATGCCAGAGGG |
MED12 |
ENSG00000184634 |
-5.50354634466085 |
[] |
[] |
-5 |
hSpCas9 |
negative selection |
3529316 |
71127015 |
71127038 |
X |
- |
26780180 |
A375 |
viability (Avana lentiCRISPRv2) |
GTAGCTGCCCACCAGATCCGAGG |
MED12 |
ENSG00000184634 |
8.4700905392688 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
3529317 |
71124258 |
71124281 |
X |
+ |
26780180 |
A375 |
viability (Avana lentiCRISPRv2) |
CTTGCACTCTCATCTCCCGAGGG |
MED12 |
ENSG00000184634 |
-1.38416615838031 |
[] |
[] |
-2 |
hSpCas9 |
negative selection |
3529318 |
71124305 |
71124328 |
X |
- |
26780180 |
A375 |
viability (Avana lentiCRISPRv2) |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
4.58570337623327 |
[] |
[] |
7 |
hSpCas9 |
negative selection |
3529319 |
71125082 |
71125105 |
X |
- |
26780180 |
A375 |
viability (Avana lentiCRISPRv2) |
CTGGTCGTAAAGAACCCCAAGGG |
MED12 |
ENSG00000184634 |
3.96320794328995 |
[] |
[] |
6 |
hSpCas9 |
negative selection |
3529320 |
71123190 |
71123213 |
X |
+ |
26780180 |
A375 |
viability (Avana lentiGuide) |
GCTCCTGGAGAAGAGACAGGCGG |
MED12 |
ENSG00000184634 |
19.9900455827919 |
[] |
[] |
8 |
hSpCas9 |
negative selection |
3637974 |
71122302 |
71122325 |
X |
+ |
26780180 |
A375 |
viability (Avana lentiGuide) |
TCCAACCTGCCCATGCCAGAGGG |
MED12 |
ENSG00000184634 |
3.07490956524462 |
[] |
[] |
3 |
hSpCas9 |
negative selection |
3637975 |
71127015 |
71127038 |
X |
- |
26780180 |
A375 |
viability (Avana lentiGuide) |
GTAGCTGCCCACCAGATCCGAGG |
MED12 |
ENSG00000184634 |
-3.88153638730012 |
[] |
[] |
-6 |
hSpCas9 |
negative selection |
3637976 |
71124258 |
71124281 |
X |
+ |
26780180 |
A375 |
viability (Avana lentiGuide) |
CTTGCACTCTCATCTCCCGAGGG |
MED12 |
ENSG00000184634 |
4.26341058991011 |
[] |
[] |
4 |
hSpCas9 |
negative selection |
3637977 |
71124305 |
71124328 |
X |
- |
26780180 |
A375 |
viability (Avana lentiGuide) |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
-7.75858959363125 |
[] |
[] |
-9 |
hSpCas9 |
negative selection |
3637978 |
71125082 |
71125105 |
X |
- |
26780180 |
A375 |
viability (Avana lentiGuide) |
CTGGTCGTAAAGAACCCCAAGGG |
MED12 |
ENSG00000184634 |
6.089689858256 |
[] |
[] |
5 |
hSpCas9 |
negative selection |
3637979 |
71123190 |
71123213 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiCRISPRv2) |
GCTCCTGGAGAAGAGACAGGCGG |
MED12 |
ENSG00000184634 |
0.9618212628257174 |
[4] |
[8,9] |
9 |
hSpCas9 |
positive selection |
3746633 |
71122302 |
71122325 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiCRISPRv2) |
TCCAACCTGCCCATGCCAGAGGG |
MED12 |
ENSG00000184634 |
1.2351827563491748 |
[4] |
[11,10] |
9 |
hSpCas9 |
positive selection |
3746634 |
71127015 |
71127038 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiCRISPRv2) |
GTAGCTGCCCACCAGATCCGAGG |
MED12 |
ENSG00000184634 |
1.5540468539068237 |
[4] |
[14,14] |
9 |
hSpCas9 |
positive selection |
3746635 |
71124258 |
71124281 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiCRISPRv2) |
CTTGCACTCTCATCTCCCGAGGG |
MED12 |
ENSG00000184634 |
1.2311487705065112 |
[5] |
[12,14] |
9 |
hSpCas9 |
positive selection |
3746636 |
71124305 |
71124328 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiCRISPRv2) |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.7081917182377924 |
[4] |
[7,8] |
9 |
hSpCas9 |
positive selection |
3746637 |
71125082 |
71125105 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiCRISPRv2) |
CTGGTCGTAAAGAACCCCAAGGG |
MED12 |
ENSG00000184634 |
1.2556524292213855 |
[5] |
[13,15] |
9 |
hSpCas9 |
positive selection |
3746638 |
71123190 |
71123213 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiGuide) |
GCTCCTGGAGAAGAGACAGGCGG |
MED12 |
ENSG00000184634 |
-1.0754305117526077 |
[4] |
[2,0] |
-8 |
hSpCas9 |
positive selection |
3855240 |
71122302 |
71122325 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiGuide) |
TCCAACCTGCCCATGCCAGAGGG |
MED12 |
ENSG00000184634 |
1.0895904669729042 |
[4] |
[6,9] |
9 |
hSpCas9 |
positive selection |
3855241 |
71127015 |
71127038 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiGuide) |
GTAGCTGCCCACCAGATCCGAGG |
MED12 |
ENSG00000184634 |
1.0278520017244925 |
[4] |
[6,11] |
9 |
hSpCas9 |
positive selection |
3855242 |
71124258 |
71124281 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiGuide) |
CTTGCACTCTCATCTCCCGAGGG |
MED12 |
ENSG00000184634 |
1.1974900655192608 |
[5] |
[12,12] |
9 |
hSpCas9 |
positive selection |
3855243 |
71124305 |
71124328 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiGuide) |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
1.0967171720995523 |
[4] |
[10,9] |
9 |
hSpCas9 |
positive selection |
3855244 |
71125082 |
71125105 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (Avana lentiGuide) |
CTGGTCGTAAAGAACCCCAAGGG |
MED12 |
ENSG00000184634 |
1.1583408869950105 |
[5] |
[12,12] |
9 |
hSpCas9 |
positive selection |
3855245 |
71120087 |
71120110 |
X |
- |
26780180 |
A375 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
1.33091662760756 |
[] |
[] |
7 |
hSpCas9 |
negative selection |
3960723 |
71119449 |
71119472 |
X |
- |
26780180 |
A375 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.257624659587523 |
[] |
[] |
0 |
hSpCas9 |
negative selection |
3960724 |
71119456 |
71119479 |
X |
+ |
26780180 |
A375 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.636493010807424 |
[] |
[] |
2 |
hSpCas9 |
negative selection |
3960725 |
71120111 |
71120134 |
X |
- |
26780180 |
A375 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
1.43396490278546 |
[] |
[] |
8 |
hSpCas9 |
negative selection |
3960726 |
71121113 |
71121136 |
X |
+ |
26780180 |
A375 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
1.08071380394979 |
[] |
[] |
5 |
hSpCas9 |
negative selection |
3960727 |
71120989 |
71121012 |
X |
- |
26780180 |
A375 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
1.07424922282899 |
[] |
[] |
5 |
hSpCas9 |
negative selection |
3960728 |
71120087 |
71120110 |
X |
- |
26780180 |
HT29 |
viability (GeCKOv2 library) |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
2.42492964134503 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
4068689 |
71119449 |
71119472 |
X |
- |
26780180 |
HT29 |
viability (GeCKOv2 library) |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
1.36271559084982 |
[] |
[] |
7 |
hSpCas9 |
negative selection |
4068690 |
71119456 |
71119479 |
X |
+ |
26780180 |
HT29 |
viability (GeCKOv2 library) |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
1.41388559918298 |
[] |
[] |
7 |
hSpCas9 |
negative selection |
4068691 |
71120111 |
71120134 |
X |
- |
26780180 |
HT29 |
viability (GeCKOv2 library) |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
2.19233683880318 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
4068692 |
71121113 |
71121136 |
X |
+ |
26780180 |
HT29 |
viability (GeCKOv2 library) |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
1.53613210243674 |
[] |
[] |
7 |
hSpCas9 |
negative selection |
4068693 |
71120989 |
71121012 |
X |
- |
26780180 |
HT29 |
viability (GeCKOv2 library) |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
2.376413709999 |
[] |
[] |
9 |
hSpCas9 |
negative selection |
4068694 |
71120087 |
71120110 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiCRISPRv1) |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
1.8733852113663685 |
[3] |
[11,10] |
9 |
hSpCas9 |
positive selection |
4151278 |
71119449 |
71119472 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiCRISPRv1) |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
1.8939001998497085 |
[3] |
[11,10] |
9 |
hSpCas9 |
positive selection |
4151279 |
71119456 |
71119479 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiCRISPRv1) |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
1.9314914514343617 |
[3] |
[10,11] |
9 |
hSpCas9 |
positive selection |
4151280 |
71120111 |
71120134 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiCRISPRv1) |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
1.8605799544041206 |
[2] |
[9,8] |
9 |
hSpCas9 |
positive selection |
4151281 |
71120087 |
71120110 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiGuide) |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
2.8776536822197687 |
[2] |
[12,10,10,10] |
9 |
hSpCas9 |
positive selection |
4215300 |
71119449 |
71119472 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiGuide) |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
2.604536732474736 |
[4] |
[12,10,12,12] |
9 |
hSpCas9 |
positive selection |
4215301 |
71119456 |
71119479 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiGuide) |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
2.5674334813919972 |
[3] |
[9,10,9,10] |
9 |
hSpCas9 |
positive selection |
4215302 |
71120111 |
71120134 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv1 lentiGuide) |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
2.5867910759485504 |
[3] |
[9,11,13,10] |
9 |
hSpCas9 |
positive selection |
4215303 |
71119449 |
71119472 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv2 lentiGuide) |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
1.619225237588385 |
[4] |
[12,12] |
9 |
hSpCas9 |
positive selection |
4282401 |
71120989 |
71121012 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv2 lentiGuide) |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
1.9158969819042724 |
[3] |
[11,11] |
9 |
hSpCas9 |
positive selection |
4282402 |
71121113 |
71121136 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv2 lentiGuide) |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
1.6910481981973926 |
[1] |
[6,6] |
9 |
hSpCas9 |
positive selection |
4282403 |
71120111 |
71120134 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv2 lentiGuide) |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
1.7584672289036045 |
[3] |
[8,10] |
9 |
hSpCas9 |
positive selection |
4346659 |
71120087 |
71120110 |
X |
- |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv2 lentiGuide) |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
2.088141317508848 |
[2] |
[8,10] |
10 |
hSpCas9 |
positive selection |
4346660 |
71119456 |
71119479 |
X |
+ |
26780180 |
A375 |
resistance to vemurafenib (GeCKOv2 lentiGuide) |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
1.6369665918103335 |
[3] |
[9,11] |
9 |
hSpCas9 |
positive selection |
4346661 |
71125101 |
71125123 |
X |
- |
27760321 |
OCIAML3 |
viability |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-2.248174080296133 |
[1066,1029] |
[178,164] |
-9 |
hSpCas9 |
negative selection |
4417529 |
71126049 |
71126071 |
X |
+ |
27760321 |
OCIAML3 |
viability |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-0.7909868787467602 |
[364,324] |
[110,213] |
-6 |
hSpCas9 |
negative selection |
4417530 |
71119857 |
71119879 |
X |
+ |
27760321 |
OCIAML3 |
viability |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-0.819054121937113 |
[179,176] |
[97,54] |
-6 |
hSpCas9 |
negative selection |
4417531 |
71127941 |
71127963 |
X |
+ |
27760321 |
OCIAML3 |
viability |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.7257397418455753 |
[566,470] |
[106,141] |
-8 |
hSpCas9 |
negative selection |
4417532 |
71128106 |
71128128 |
X |
- |
27760321 |
OCIAML3 |
viability |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-1.1420282335297873 |
[574,436] |
[140,225] |
-7 |
hSpCas9 |
negative selection |
4417533 |
71125101 |
71125123 |
X |
- |
27760321 |
OCIAML2 |
viability |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-2.2336716506890006 |
[1066,1029] |
[165,199] |
-9 |
hSpCas9 |
negative selection |
4500992 |
71126049 |
71126071 |
X |
+ |
27760321 |
OCIAML2 |
viability |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-0.9110753241239706 |
[364,324] |
[139,158] |
-7 |
hSpCas9 |
negative selection |
4500993 |
71119857 |
71119879 |
X |
+ |
27760321 |
OCIAML2 |
viability |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-1.51147258660482 |
[179,176] |
[61,35] |
-8 |
hSpCas9 |
negative selection |
4500994 |
71127941 |
71127963 |
X |
+ |
27760321 |
OCIAML2 |
viability |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.1155160684540313 |
[566,470] |
[201,180] |
-8 |
hSpCas9 |
negative selection |
4500995 |
71128106 |
71128128 |
X |
- |
27760321 |
OCIAML2 |
viability |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.5038030355112217 |
[574,436] |
[269,307] |
-5 |
hSpCas9 |
negative selection |
4500996 |
71125101 |
71125123 |
X |
- |
27760321 |
MV411 |
viability |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-1.160221022274814 |
[1066,1029] |
[258,386] |
-6 |
hSpCas9 |
negative selection |
4584455 |
71126049 |
71126071 |
X |
+ |
27760321 |
MV411 |
viability |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-1.691046270662043 |
[364,324] |
[75,61] |
-8 |
hSpCas9 |
negative selection |
4584456 |
71119857 |
71119879 |
X |
+ |
27760321 |
MV411 |
viability |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-1.4176810065644212 |
[179,176] |
[50,33] |
-7 |
hSpCas9 |
negative selection |
4584457 |
71127941 |
71127963 |
X |
+ |
27760321 |
MV411 |
viability |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-0.1436926981449888 |
[566,470] |
[410,154] |
-1 |
hSpCas9 |
negative selection |
4584458 |
71128106 |
71128128 |
X |
- |
27760321 |
MV411 |
viability |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-2.071898662736 |
[574,436] |
[67,94] |
-8 |
hSpCas9 |
negative selection |
4584459 |
71125101 |
71125123 |
X |
- |
27760321 |
HL60 |
viability |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-0.89081050126701 |
[1066,1029] |
[686,224] |
-7 |
hSpCas9 |
negative selection |
4667918 |
71126049 |
71126071 |
X |
+ |
27760321 |
HL60 |
viability |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-0.9004708871416125 |
[364,324] |
[125,176] |
-7 |
hSpCas9 |
negative selection |
4667919 |
71119857 |
71119879 |
X |
+ |
27760321 |
HL60 |
viability |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-0.7233881086573619 |
[179,176] |
[89,86] |
-6 |
hSpCas9 |
negative selection |
4667920 |
71127941 |
71127963 |
X |
+ |
27760321 |
HL60 |
viability |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-0.8779285609128633 |
[566,470] |
[252,204] |
-7 |
hSpCas9 |
negative selection |
4667921 |
71128106 |
71128128 |
X |
- |
27760321 |
HL60 |
viability |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-1.5286217949571785 |
[574,436] |
[129,154] |
-8 |
hSpCas9 |
negative selection |
4667922 |
71125101 |
71125123 |
X |
- |
27760321 |
HT1080 |
viability |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-1.0620506452274694 |
[1029,803] |
[110,244] |
-4 |
hSpCas9 |
negative selection |
4751381 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT1080 |
viability |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
0.9793232627999146 |
[324,253] |
[182,275] |
5 |
hSpCas9 |
negative selection |
4751382 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT1080 |
viability |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
2.982116627067768 |
[176,137] |
[468,524] |
9 |
hSpCas9 |
negative selection |
4751383 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT1080 |
viability |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
0.785553821077989 |
[470,367] |
[36,562] |
4 |
hSpCas9 |
negative selection |
4751384 |
71128106 |
71128128 |
X |
- |
27760321 |
HT1080 |
viability |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
1.3634690078883895 |
[436,340] |
[255,554] |
7 |
hSpCas9 |
negative selection |
4751385 |
71125101 |
71125123 |
X |
- |
27760321 |
HT29 |
viability after 7 days |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-1.8938804541882486 |
[1029,803] |
[383,360,218] |
-9 |
hSpCas9 |
negative selection |
4834844 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT29 |
viability after 7 days |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-0.44819367491724993 |
[324,253] |
[183,333,286] |
-6 |
hSpCas9 |
negative selection |
4834845 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT29 |
viability after 7 days |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
0.20323290192061805 |
[176,137] |
[311,124,271] |
3 |
hSpCas9 |
negative selection |
4834846 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT29 |
viability after 7 days |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-0.9058775967974281 |
[470,367] |
[271,238,347] |
-8 |
hSpCas9 |
negative selection |
4834847 |
71128106 |
71128128 |
X |
- |
27760321 |
HT29 |
viability after 7 days |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.5235314738003282 |
[436,340] |
[307,362,365] |
-6 |
hSpCas9 |
negative selection |
4834848 |
71125101 |
71125123 |
X |
- |
27760321 |
HT29 |
viability after 25 days |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-5.376356386456322 |
[1029,803] |
[0,17,61] |
-9 |
hSpCas9 |
negative selection |
4918307 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT29 |
viability after 25 days |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-0.6421003444919595 |
[324,253] |
[174,242,220] |
-5 |
hSpCas9 |
negative selection |
4918308 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT29 |
viability after 25 days |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-2.8557370625421523 |
[176,137] |
[24,37,9] |
-8 |
hSpCas9 |
negative selection |
4918309 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT29 |
viability after 25 days |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-2.1427285285571465 |
[470,367] |
[94,65,171] |
-8 |
hSpCas9 |
negative selection |
4918310 |
71128106 |
71128128 |
X |
- |
27760321 |
HT29 |
viability after 25 days |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.4801614974303325 |
[436,340] |
[328,418,193] |
-4 |
hSpCas9 |
negative selection |
4918311 |
71125101 |
71125123 |
X |
- |
27760321 |
HT29 |
viability after 22 days |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-4.416557887055275 |
[1029,803] |
[7,96,44] |
-9 |
hSpCas9 |
negative selection |
5001770 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT29 |
viability after 22 days |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-1.8401573865514336 |
[324,253] |
[136,75,65] |
-8 |
hSpCas9 |
negative selection |
5001771 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT29 |
viability after 22 days |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-2.3923305869684173 |
[176,137] |
[33,40,28] |
-8 |
hSpCas9 |
negative selection |
5001772 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT29 |
viability after 22 days |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.664505381712498 |
[470,367] |
[141,87,229] |
-7 |
hSpCas9 |
negative selection |
5001773 |
71128106 |
71128128 |
X |
- |
27760321 |
HT29 |
viability after 22 days |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.7651828325941226 |
[436,340] |
[380,209,198] |
-6 |
hSpCas9 |
negative selection |
5001774 |
71125101 |
71125123 |
X |
- |
27760321 |
HT29 |
viability after 19 days |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-3.9679862059976063 |
[1029,803] |
[50,125,23] |
-9 |
hSpCas9 |
negative selection |
5085233 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT29 |
viability after 19 days |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-0.9797129816279629 |
[324,253] |
[140,277,84] |
-6 |
hSpCas9 |
negative selection |
5085234 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT29 |
viability after 19 days |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-2.3226295062242084 |
[176,137] |
[3,100,0] |
-8 |
hSpCas9 |
negative selection |
5085235 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT29 |
viability after 19 days |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.3034999965008935 |
[470,367] |
[139,340,99] |
-7 |
hSpCas9 |
negative selection |
5085236 |
71128106 |
71128128 |
X |
- |
27760321 |
HT29 |
viability after 19 days |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.5955496139025442 |
[436,340] |
[246,601,38] |
-5 |
hSpCas9 |
negative selection |
5085237 |
71125101 |
71125123 |
X |
- |
27760321 |
HT29 |
viability after 16 days |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-4.618682341468249 |
[1029,803] |
[104,12,13] |
-9 |
hSpCas9 |
negative selection |
5168696 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT29 |
viability after 16 days |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-2.0480328231077793 |
[324,253] |
[65,70,96] |
-8 |
hSpCas9 |
negative selection |
5168697 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT29 |
viability after 16 days |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-0.5847472769339939 |
[176,137] |
[29,123,189] |
-5 |
hSpCas9 |
negative selection |
5168698 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT29 |
viability after 16 days |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.834095505986493 |
[470,367] |
[103,142,144] |
-8 |
hSpCas9 |
negative selection |
5168699 |
71128106 |
71128128 |
X |
- |
27760321 |
HT29 |
viability after 16 days |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.8546274012124836 |
[436,340] |
[284,208,232] |
-6 |
hSpCas9 |
negative selection |
5168700 |
71125101 |
71125123 |
X |
- |
27760321 |
HT29 |
viability after 13 days |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-3.710391381734199 |
[1029,803] |
[27,135,79] |
-9 |
hSpCas9 |
negative selection |
5252159 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT29 |
viability after 13 days |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-0.7223360511118603 |
[324,253] |
[147,244,216] |
-6 |
hSpCas9 |
negative selection |
5252160 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT29 |
viability after 13 days |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-2.399002756941207 |
[176,137] |
[16,18,65] |
-9 |
hSpCas9 |
negative selection |
5252161 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT29 |
viability after 13 days |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.4818947106063936 |
[470,367] |
[161,190,169] |
-8 |
hSpCas9 |
negative selection |
5252162 |
71128106 |
71128128 |
X |
- |
27760321 |
HT29 |
viability after 13 days |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.8513202986282794 |
[436,340] |
[370,195,186] |
-7 |
hSpCas9 |
negative selection |
5252163 |
71125101 |
71125123 |
X |
- |
27760321 |
HT29 |
viability after 10 days |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-2.218965578080126 |
[1029,803] |
[350,143,239] |
-9 |
hSpCas9 |
negative selection |
5335622 |
71126049 |
71126071 |
X |
+ |
27760321 |
HT29 |
viability after 10 days |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-1.0611017357293773 |
[324,253] |
[181,174,162] |
-8 |
hSpCas9 |
negative selection |
5335623 |
71119857 |
71119879 |
X |
+ |
27760321 |
HT29 |
viability after 10 days |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
-0.6043789945877949 |
[176,137] |
[174,68,141] |
-6 |
hSpCas9 |
negative selection |
5335624 |
71127941 |
71127963 |
X |
+ |
27760321 |
HT29 |
viability after 10 days |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.0200679946093438 |
[470,367] |
[126,400,250] |
-8 |
hSpCas9 |
negative selection |
5335625 |
71128106 |
71128128 |
X |
- |
27760321 |
HT29 |
viability after 10 days |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
-0.5185369785566274 |
[436,340] |
[170,572,280] |
-6 |
hSpCas9 |
negative selection |
5335626 |
71125101 |
71125123 |
X |
- |
27760321 |
MOLM13 |
viability |
GTACTGCACGTGTCGTGGCTGG |
MED12 |
ENSG00000184634 |
-2.7672126231560012 |
[1066,1029] |
[45,121] |
-8 |
hSpCas9 |
negative selection |
5419085 |
71126049 |
71126071 |
X |
+ |
27760321 |
MOLM13 |
viability |
GCAGAAGCGGCGACGCAACCGG |
MED12 |
ENSG00000184634 |
-2.4595481943977227 |
[364,324] |
[50,21] |
-8 |
hSpCas9 |
negative selection |
5419086 |
71119857 |
71119879 |
X |
+ |
27760321 |
MOLM13 |
viability |
CTCACGCAACTAGCCAAAAAGG |
MED12 |
ENSG00000184634 |
1.3747886610807334 |
[179,176] |
[41,448] |
8 |
hSpCas9 |
negative selection |
5419087 |
71127941 |
71127963 |
X |
+ |
27760321 |
MOLM13 |
viability |
ATCGGAATCAAATATGCGCTGG |
MED12 |
ENSG00000184634 |
-1.8791600615403916 |
[566,470] |
[21,127] |
-7 |
hSpCas9 |
negative selection |
5419088 |
71128106 |
71128128 |
X |
- |
27760321 |
MOLM13 |
viability |
CCCATACCTATCGGGATCATGG |
MED12 |
ENSG00000184634 |
0.1530660881749739 |
[574,436] |
[362,273] |
1 |
hSpCas9 |
negative selection |
5419089 |
71118629 |
71118652 |
X |
- |
27661255 |
K562 |
viability |
GCGGCCGAGAGACAACAAGGGGG |
MED12 |
ENSG00000184634 |
-0.18904671328331113 |
[165,276] |
[169,139] |
-6 |
dCas9-KRAB |
negative selection |
5492787 |
71118648 |
71118671 |
X |
- |
27661255 |
K562 |
viability |
GGCGGTGGTTGAGAGGACGGCGG |
MED12 |
ENSG00000184634 |
-1.282698382359761 |
[927,790] |
[336,236] |
-9 |
dCas9-KRAB |
negative selection |
5492788 |
71118670 |
71118693 |
X |
- |
27661255 |
K562 |
viability |
GGGAGAGGGAGCCGAAAAGGGGG |
MED12 |
ENSG00000184634 |
-1.6760331121674739 |
[1428,1285] |
[400,287] |
-9 |
dCas9-KRAB |
negative selection |
5492789 |
71118692 |
71118715 |
X |
- |
27661255 |
K562 |
viability |
GCTGACTGGGGGAACGGGAAGGG |
MED12 |
ENSG00000184634 |
-1.5756423546648013 |
[477,353] |
[137,89] |
-9 |
dCas9-KRAB |
negative selection |
5492790 |
71119449 |
71119472 |
X |
- |
27260156 |
BXPC3 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.36598961349461145 |
[1672] |
[1216,1226,1348,1690] |
-7 |
hSpCas9 |
negative selection |
5554861 |
71120989 |
71121012 |
X |
- |
27260156 |
BXPC3 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.5791544549348145 |
[600] |
[330,419,437,511] |
-8 |
hSpCas9 |
negative selection |
5554862 |
71121113 |
71121136 |
X |
+ |
27260156 |
BXPC3 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.06460094605634148 |
[175] |
[130,179,188,211] |
-1 |
hSpCas9 |
negative selection |
5554863 |
71120111 |
71120134 |
X |
- |
27260156 |
BXPC3 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.46055135375549167 |
[517] |
[322,429,379,450] |
-7 |
hSpCas9 |
negative selection |
5619119 |
71120087 |
71120110 |
X |
- |
27260156 |
BXPC3 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.49508066503582215 |
[244] |
[166,182,199,176] |
-8 |
hSpCas9 |
negative selection |
5619120 |
71119456 |
71119479 |
X |
+ |
27260156 |
BXPC3 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.3917980185967884 |
[890] |
[586,632,812,837] |
-7 |
hSpCas9 |
negative selection |
5619121 |
71119449 |
71119472 |
X |
- |
27260156 |
A673 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.3140877348033957 |
[1672] |
[1699,1427,1621,1730] |
-6 |
hSpCas9 |
negative selection |
5676112 |
71120989 |
71121012 |
X |
- |
27260156 |
A673 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.5148773576452829 |
[600] |
[552,435,491,547] |
-8 |
hSpCas9 |
negative selection |
5676113 |
71121113 |
71121136 |
X |
+ |
27260156 |
A673 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.14033439458986674 |
[175] |
[280,188,168,134] |
-3 |
hSpCas9 |
negative selection |
5676114 |
71120111 |
71120134 |
X |
- |
27260156 |
A673 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.5802368029683347 |
[517] |
[517,349,420,385] |
-8 |
hSpCas9 |
negative selection |
5740370 |
71120087 |
71120110 |
X |
- |
27260156 |
A673 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.3879750861821807 |
[244] |
[274,243,155,229] |
-7 |
hSpCas9 |
negative selection |
5740371 |
71119456 |
71119479 |
X |
+ |
27260156 |
A673 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.22104188096481192 |
[890] |
[916,949,825,979] |
-5 |
hSpCas9 |
negative selection |
5740372 |
71119449 |
71119472 |
X |
- |
27260156 |
A375 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.11830678919145132 |
[1672] |
[2278,2404,2020,1844] |
1 |
hSpCas9 |
negative selection |
5797363 |
71120989 |
71121012 |
X |
- |
27260156 |
A375 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.3494062431585005 |
[600] |
[432,724,616,460] |
-5 |
hSpCas9 |
negative selection |
5797364 |
71121113 |
71121136 |
X |
+ |
27260156 |
A375 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.38137049029243575 |
[175] |
[199,159,184,93] |
-5 |
hSpCas9 |
negative selection |
5797365 |
71120111 |
71120134 |
X |
- |
27260156 |
A375 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.28501979834451796 |
[517] |
[638,563,417,386] |
-4 |
hSpCas9 |
negative selection |
5861621 |
71120087 |
71120110 |
X |
- |
27260156 |
A375 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.1641696948068705 |
[244] |
[284,375,291,102] |
-2 |
hSpCas9 |
negative selection |
5861622 |
71119456 |
71119479 |
X |
+ |
27260156 |
A375 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.03196328869222842 |
[890] |
[1091,1324,945,776] |
0 |
hSpCas9 |
negative selection |
5861623 |
71119449 |
71119472 |
X |
- |
27260156 |
COLO741 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.1732887925048059 |
[1672] |
[2118,1808,1781] |
-4 |
hSpCas9 |
negative selection |
5918614 |
71120989 |
71121012 |
X |
- |
27260156 |
COLO741 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.3817685815066413 |
[600] |
[625,626,521] |
-7 |
hSpCas9 |
negative selection |
5918615 |
71121113 |
71121136 |
X |
+ |
27260156 |
COLO741 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.01956838013982165 |
[175] |
[158,267,248] |
0 |
hSpCas9 |
negative selection |
5918616 |
71120111 |
71120134 |
X |
- |
27260156 |
COLO741 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.39819837810569475 |
[517] |
[623,603,302] |
-7 |
hSpCas9 |
negative selection |
5982872 |
71120087 |
71120110 |
X |
- |
27260156 |
COLO741 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.48000101977199705 |
[244] |
[278,224,176] |
-7 |
hSpCas9 |
negative selection |
5982873 |
71119456 |
71119479 |
X |
+ |
27260156 |
COLO741 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.08407898181180762 |
[890] |
[1295,1119,839] |
-2 |
hSpCas9 |
negative selection |
5982874 |
71119449 |
71119472 |
X |
- |
27260156 |
CAL120 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.3682666169829709 |
[1672] |
[3345,2193,2620] |
5 |
hSpCas9 |
negative selection |
6039865 |
71120989 |
71121012 |
X |
- |
27260156 |
CAL120 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
0.5638198887202492 |
[600] |
[1023,1466,817] |
8 |
hSpCas9 |
negative selection |
6039866 |
71121113 |
71121136 |
X |
+ |
27260156 |
CAL120 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.2616838967009445 |
[175] |
[367,258,177] |
4 |
hSpCas9 |
negative selection |
6039867 |
71120111 |
71120134 |
X |
- |
27260156 |
CAL120 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.04608214308082584 |
[517] |
[915,453,547] |
0 |
hSpCas9 |
negative selection |
6104123 |
71120087 |
71120110 |
X |
- |
27260156 |
CAL120 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.41933271233950253 |
[244] |
[234,227,221] |
-6 |
hSpCas9 |
negative selection |
6104124 |
71119456 |
71119479 |
X |
+ |
27260156 |
CAL120 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.09949051942916687 |
[890] |
[1140,993,1416] |
1 |
hSpCas9 |
negative selection |
6104125 |
71119449 |
71119472 |
X |
- |
27260156 |
CADOES1 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.4412798412884942 |
[1672] |
[1150,1002,1040,1397] |
-6 |
hSpCas9 |
negative selection |
6161116 |
71120989 |
71121012 |
X |
- |
27260156 |
CADOES1 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.136213743489351 |
[600] |
[264,244,256,249] |
-9 |
hSpCas9 |
negative selection |
6161117 |
71121113 |
71121136 |
X |
+ |
27260156 |
CADOES1 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.1333842832481349 |
[175] |
[48,404,161,99] |
2 |
hSpCas9 |
negative selection |
6161118 |
71120111 |
71120134 |
X |
- |
27260156 |
CADOES1 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.31774560715650396 |
[517] |
[374,429,386,352] |
-5 |
hSpCas9 |
negative selection |
6225374 |
71120087 |
71120110 |
X |
- |
27260156 |
CADOES1 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.2396232301347052 |
[244] |
[227,255,95,191] |
-4 |
hSpCas9 |
negative selection |
6225375 |
71119456 |
71119479 |
X |
+ |
27260156 |
CADOES1 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.31964706825732014 |
[890] |
[648,567,743,695] |
-5 |
hSpCas9 |
negative selection |
6225376 |
71119449 |
71119472 |
X |
- |
27260156 |
EWS502 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.5487442501017359 |
[1672] |
[1155,1278,1222,1184] |
-7 |
hSpCas9 |
negative selection |
6282367 |
71120989 |
71121012 |
X |
- |
27260156 |
EWS502 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.589857919747616 |
[600] |
[255,207,229,140] |
-9 |
hSpCas9 |
negative selection |
6282368 |
71121113 |
71121136 |
X |
+ |
27260156 |
EWS502 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.18954150504505884 |
[175] |
[206,124,175,139] |
-3 |
hSpCas9 |
negative selection |
6282369 |
71120111 |
71120134 |
X |
- |
27260156 |
EWS502 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.31647974003297286 |
[517] |
[383,410,421,559] |
-5 |
hSpCas9 |
negative selection |
6346625 |
71120087 |
71120110 |
X |
- |
27260156 |
EWS502 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.4195676287725789 |
[244] |
[220,176,172,201] |
-6 |
hSpCas9 |
negative selection |
6346626 |
71119456 |
71119479 |
X |
+ |
27260156 |
EWS502 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.47627738323999697 |
[890] |
[598,683,814,619] |
-7 |
hSpCas9 |
negative selection |
6346627 |
71119449 |
71119472 |
X |
- |
27260156 |
EW8 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.3024009229960287 |
[1672] |
[1148,898,1114,1232] |
-5 |
hSpCas9 |
negative selection |
6403618 |
71120989 |
71121012 |
X |
- |
27260156 |
EW8 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.6281758841708749 |
[600] |
[297,336,199,441] |
-8 |
hSpCas9 |
negative selection |
6403619 |
71121113 |
71121136 |
X |
+ |
27260156 |
EW8 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.5335340548008498 |
[175] |
[160,96,55,93] |
-7 |
hSpCas9 |
negative selection |
6403620 |
71120111 |
71120134 |
X |
- |
27260156 |
EW8 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.13143279333394323 |
[517] |
[429,318,320,476] |
-2 |
hSpCas9 |
negative selection |
6467876 |
71120087 |
71120110 |
X |
- |
27260156 |
EW8 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.39396664220602984 |
[244] |
[346,256,203,253] |
7 |
hSpCas9 |
negative selection |
6467877 |
71119456 |
71119479 |
X |
+ |
27260156 |
EW8 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.05882908036234247 |
[890] |
[870,844,573,521] |
-1 |
hSpCas9 |
negative selection |
6467878 |
71119449 |
71119472 |
X |
- |
27260156 |
CORL105 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.16499532514072368 |
[1672] |
[2430,1663,2508,2245] |
3 |
hSpCas9 |
negative selection |
6524869 |
71120989 |
71121012 |
X |
- |
27260156 |
CORL105 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
0.30890092764950167 |
[600] |
[950,933,964,652] |
6 |
hSpCas9 |
negative selection |
6524870 |
71121113 |
71121136 |
X |
+ |
27260156 |
CORL105 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.38336927596681614 |
[175] |
[270,271,293,241] |
7 |
hSpCas9 |
negative selection |
6524871 |
71120111 |
71120134 |
X |
- |
27260156 |
CORL105 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.21313540214857501 |
[517] |
[659,515,599,333] |
-4 |
hSpCas9 |
negative selection |
6589127 |
71120087 |
71120110 |
X |
- |
27260156 |
CORL105 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.3308510306191692 |
[244] |
[215,279,197,211] |
-6 |
hSpCas9 |
negative selection |
6589128 |
71119456 |
71119479 |
X |
+ |
27260156 |
CORL105 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.46376905306036353 |
[890] |
[1453,1398,1657,1278] |
8 |
hSpCas9 |
negative selection |
6589129 |
71119449 |
71119472 |
X |
- |
27260156 |
HS294T |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.21766033870964407 |
[1672] |
[503,997,587,967] |
3 |
hSpCas9 |
negative selection |
6646120 |
71120989 |
71121012 |
X |
- |
27260156 |
HS294T |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.6123828089795751 |
[600] |
[151,117,159,183] |
-7 |
hSpCas9 |
negative selection |
6646121 |
71121113 |
71121136 |
X |
+ |
27260156 |
HS294T |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.3228390111502595 |
[175] |
[81,20,42,72] |
-4 |
hSpCas9 |
negative selection |
6646122 |
71120111 |
71120134 |
X |
- |
27260156 |
HS294T |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.013148263647499658 |
[517] |
[167,152,246,235] |
0 |
hSpCas9 |
negative selection |
6710378 |
71120087 |
71120110 |
X |
- |
27260156 |
HS294T |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.42459616192858896 |
[244] |
[52,51,80,103] |
-6 |
hSpCas9 |
negative selection |
6710379 |
71119456 |
71119479 |
X |
+ |
27260156 |
HS294T |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.6532989914331127 |
[890] |
[373,895,335,567] |
8 |
hSpCas9 |
negative selection |
6710380 |
71119449 |
71119472 |
X |
- |
27260156 |
HCC44 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.6056337405405319 |
[1672] |
[2875,2463,3745,2623] |
8 |
hSpCas9 |
negative selection |
6767371 |
71120989 |
71121012 |
X |
- |
27260156 |
HCC44 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
0.162667752828687 |
[600] |
[732,605,1014,746] |
2 |
hSpCas9 |
negative selection |
6767372 |
71121113 |
71121136 |
X |
+ |
27260156 |
HCC44 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.11814206410509343 |
[175] |
[321,71,169,193] |
-2 |
hSpCas9 |
negative selection |
6767373 |
71120111 |
71120134 |
X |
- |
27260156 |
HCC44 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
0.2810108847396195 |
[517] |
[683,515,1072,657] |
4 |
hSpCas9 |
negative selection |
6831629 |
71120087 |
71120110 |
X |
- |
27260156 |
HCC44 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.4109529951769171 |
[244] |
[447,293,216,498] |
6 |
hSpCas9 |
negative selection |
6831630 |
71119456 |
71119479 |
X |
+ |
27260156 |
HCC44 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.23176350538226642 |
[890] |
[1367,910,1303,1215] |
4 |
hSpCas9 |
negative selection |
6831631 |
71119449 |
71119472 |
X |
- |
27260156 |
G402 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.512820073753989 |
[1672] |
[1884,1768,1150,1017] |
-6 |
hSpCas9 |
negative selection |
6888622 |
71120989 |
71121012 |
X |
- |
27260156 |
G402 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.2787957978890598 |
[600] |
[225,379,74,509] |
-8 |
hSpCas9 |
negative selection |
6888623 |
71121113 |
71121136 |
X |
+ |
27260156 |
G402 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.3228093617715395 |
[175] |
[153,290,277,331] |
4 |
hSpCas9 |
negative selection |
6888624 |
71120111 |
71120134 |
X |
- |
27260156 |
G402 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.2917320471300625 |
[517] |
[736,401,462,487] |
-4 |
hSpCas9 |
negative selection |
6952880 |
71120087 |
71120110 |
X |
- |
27260156 |
G402 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.1067778148625349 |
[244] |
[145,623,93,247] |
-1 |
hSpCas9 |
negative selection |
6952881 |
71119456 |
71119479 |
X |
+ |
27260156 |
G402 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.847740230465059 |
[890] |
[636,662,533,588] |
-7 |
hSpCas9 |
negative selection |
6952882 |
71119449 |
71119472 |
X |
- |
27260156 |
L33 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.1447894610467706 |
[1672] |
[1716,786,1153,1926] |
3 |
hSpCas9 |
negative selection |
7009873 |
71120989 |
71121012 |
X |
- |
27260156 |
L33 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
0.13062442397081137 |
[600] |
[550,237,422,827] |
3 |
hSpCas9 |
negative selection |
7009874 |
71121113 |
71121136 |
X |
+ |
27260156 |
L33 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.19146385170645175 |
[175] |
[167,58,94,152] |
-4 |
hSpCas9 |
negative selection |
7009875 |
71120111 |
71120134 |
X |
- |
27260156 |
L33 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.10341743029594952 |
[517] |
[476,171,364,451] |
-2 |
hSpCas9 |
negative selection |
7074131 |
71120087 |
71120110 |
X |
- |
27260156 |
L33 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.5042438527672017 |
[244] |
[188,80,127,100] |
-8 |
hSpCas9 |
negative selection |
7074132 |
71119456 |
71119479 |
X |
+ |
27260156 |
L33 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.36256760219359707 |
[890] |
[1198,455,757,1063] |
7 |
hSpCas9 |
negative selection |
7074133 |
71119449 |
71119472 |
X |
- |
27260156 |
K562 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.47610669438677555 |
[1672] |
[2318,2195,1619,2135] |
6 |
hSpCas9 |
negative selection |
7131124 |
71120989 |
71121012 |
X |
- |
27260156 |
K562 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.6381517146829303 |
[600] |
[173,156,274,87] |
-9 |
hSpCas9 |
negative selection |
7131125 |
71121113 |
71121136 |
X |
+ |
27260156 |
K562 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-1.1922377737338454 |
[175] |
[135,51,79,15] |
-8 |
hSpCas9 |
negative selection |
7131126 |
71120111 |
71120134 |
X |
- |
27260156 |
K562 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
0.11782798410807593 |
[517] |
[583,561,486,383] |
1 |
hSpCas9 |
negative selection |
7195382 |
71120087 |
71120110 |
X |
- |
27260156 |
K562 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.5467791253715619 |
[244] |
[108,143,64,259] |
-6 |
hSpCas9 |
negative selection |
7195383 |
71119456 |
71119479 |
X |
+ |
27260156 |
K562 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.3526077837356165 |
[890] |
[734,255,705,751] |
-4 |
hSpCas9 |
negative selection |
7195384 |
71119449 |
71119472 |
X |
- |
27260156 |
HT29 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.7656957662399524 |
[1672] |
[1295,1312,1215,993] |
-8 |
hSpCas9 |
negative selection |
7252375 |
71120989 |
71121012 |
X |
- |
27260156 |
HT29 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.7885674808823855 |
[600] |
[197,235,249,166] |
-9 |
hSpCas9 |
negative selection |
7252376 |
71121113 |
71121136 |
X |
+ |
27260156 |
HT29 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.29434848462707786 |
[175] |
[218,116,192,166] |
-5 |
hSpCas9 |
negative selection |
7252377 |
71120111 |
71120134 |
X |
- |
27260156 |
HT29 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.33327405770193386 |
[517] |
[543,479,515,461] |
-6 |
hSpCas9 |
negative selection |
7316633 |
71120087 |
71120110 |
X |
- |
27260156 |
HT29 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.0692195734781207 |
[244] |
[178,178,128,91] |
-9 |
hSpCas9 |
negative selection |
7316634 |
71119456 |
71119479 |
X |
+ |
27260156 |
HT29 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.5350571396280529 |
[890] |
[755,818,755,669] |
-7 |
hSpCas9 |
negative selection |
7316635 |
71119449 |
71119472 |
X |
- |
27260156 |
MHHES1 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.7821585229967016 |
[1672] |
[1121,1189,991,1070] |
-8 |
hSpCas9 |
negative selection |
7373626 |
71120989 |
71121012 |
X |
- |
27260156 |
MHHES1 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.7545876117620349 |
[600] |
[360,389,509,342] |
-8 |
hSpCas9 |
negative selection |
7373627 |
71121113 |
71121136 |
X |
+ |
27260156 |
MHHES1 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.5502197574222738 |
[175] |
[232,59,172,87] |
-8 |
hSpCas9 |
negative selection |
7373628 |
71120111 |
71120134 |
X |
- |
27260156 |
MHHES1 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.5799163700496652 |
[517] |
[437,436,301,385] |
-8 |
hSpCas9 |
negative selection |
7437884 |
71120087 |
71120110 |
X |
- |
27260156 |
MHHES1 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.6880338468735627 |
[244] |
[193,264,124,120] |
-8 |
hSpCas9 |
negative selection |
7437885 |
71119456 |
71119479 |
X |
+ |
27260156 |
MHHES1 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.2092138810855927 |
[890] |
[1042,1075,738,679] |
-4 |
hSpCas9 |
negative selection |
7437886 |
71119449 |
71119472 |
X |
- |
27260156 |
MEWO |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.22621630003139015 |
[1672] |
[1642,1115,1314] |
-5 |
hSpCas9 |
negative selection |
7494877 |
71120989 |
71121012 |
X |
- |
27260156 |
MEWO |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.1587533278887323 |
[600] |
[213,279,253] |
-9 |
hSpCas9 |
negative selection |
7494878 |
71121113 |
71121136 |
X |
+ |
27260156 |
MEWO |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.33489103401991827 |
[175] |
[116,128,142] |
-6 |
hSpCas9 |
negative selection |
7494879 |
71120111 |
71120134 |
X |
- |
27260156 |
MEWO |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.4015933229482698 |
[517] |
[368,353,377] |
-7 |
hSpCas9 |
negative selection |
7559135 |
71120087 |
71120110 |
X |
- |
27260156 |
MEWO |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.17624218380165924 |
[244] |
[219,169,221] |
-4 |
hSpCas9 |
negative selection |
7559136 |
71119456 |
71119479 |
X |
+ |
27260156 |
MEWO |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.47093141872161826 |
[890] |
[603,735,463] |
-7 |
hSpCas9 |
negative selection |
7559137 |
71119449 |
71119472 |
X |
- |
27260156 |
LNCAPCLONEFGC |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.6731676855355473 |
[1672] |
[929,862,955,1058] |
-7 |
hSpCas9 |
negative selection |
7616128 |
71120989 |
71121012 |
X |
- |
27260156 |
LNCAPCLONEFGC |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.7237079169676045 |
[600] |
[226,397,464,245] |
-8 |
hSpCas9 |
negative selection |
7616129 |
71121113 |
71121136 |
X |
+ |
27260156 |
LNCAPCLONEFGC |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.07222520646283948 |
[175] |
[95,272,121,166] |
1 |
hSpCas9 |
negative selection |
7616130 |
71120111 |
71120134 |
X |
- |
27260156 |
LNCAPCLONEFGC |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.09323442669714468 |
[517] |
[353,298,458,660] |
-1 |
hSpCas9 |
negative selection |
7680386 |
71120087 |
71120110 |
X |
- |
27260156 |
LNCAPCLONEFGC |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.2792432469360515 |
[244] |
[160,164,101,292] |
-4 |
hSpCas9 |
negative selection |
7680387 |
71119456 |
71119479 |
X |
+ |
27260156 |
LNCAPCLONEFGC |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.47233336296688583 |
[890] |
[502,455,712,683] |
-6 |
hSpCas9 |
negative selection |
7680388 |
71119449 |
71119472 |
X |
- |
27260156 |
PANC0327 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.07700872466101605 |
[1672] |
[1350,1741,1676,1459] |
1 |
hSpCas9 |
negative selection |
7737379 |
71120989 |
71121012 |
X |
- |
27260156 |
PANC0327 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.0593134830909787 |
[600] |
[280,139,415,204] |
-8 |
hSpCas9 |
negative selection |
7737380 |
71121113 |
71121136 |
X |
+ |
27260156 |
PANC0327 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.30329660687014703 |
[175] |
[89,215,125,327] |
4 |
hSpCas9 |
negative selection |
7737381 |
71120111 |
71120134 |
X |
- |
27260156 |
PANC0327 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.38276887329875037 |
[517] |
[357,234,309,523] |
-5 |
hSpCas9 |
negative selection |
7801637 |
71120087 |
71120110 |
X |
- |
27260156 |
PANC0327 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.555900098153816 |
[244] |
[166,130,198,98] |
-7 |
hSpCas9 |
negative selection |
7801638 |
71119456 |
71119479 |
X |
+ |
27260156 |
PANC0327 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.039273428046141534 |
[890] |
[755,779,665,875] |
0 |
hSpCas9 |
negative selection |
7801639 |
71119449 |
71119472 |
X |
- |
27260156 |
NCIH2009 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.4965952779999325 |
[1672] |
[2036,1630,1374] |
-6 |
hSpCas9 |
negative selection |
7858630 |
71120989 |
71121012 |
X |
- |
27260156 |
NCIH2009 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.8603162780043088 |
[600] |
[482,398,509] |
-8 |
hSpCas9 |
negative selection |
7858631 |
71121113 |
71121136 |
X |
+ |
27260156 |
NCIH2009 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.24041121472342186 |
[175] |
[311,77,256] |
-3 |
hSpCas9 |
negative selection |
7858632 |
71120111 |
71120134 |
X |
- |
27260156 |
NCIH2009 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.18888989696218925 |
[517] |
[844,644,454] |
-3 |
hSpCas9 |
negative selection |
7922888 |
71120087 |
71120110 |
X |
- |
27260156 |
NCIH2009 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.1522160489248658 |
[244] |
[213,133,125] |
-8 |
hSpCas9 |
negative selection |
7922889 |
71119456 |
71119479 |
X |
+ |
27260156 |
NCIH2009 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.1335931178005948 |
[890] |
[1298,1125,1009] |
-2 |
hSpCas9 |
negative selection |
7922890 |
71119449 |
71119472 |
X |
- |
27260156 |
NCIH1373 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.3815742616101465 |
[1672] |
[1351,1006,1809,424] |
-4 |
hSpCas9 |
negative selection |
7979881 |
71120989 |
71121012 |
X |
- |
27260156 |
NCIH1373 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.9089438044897207 |
[600] |
[178,168,186,47] |
-9 |
hSpCas9 |
negative selection |
7979882 |
71121113 |
71121136 |
X |
+ |
27260156 |
NCIH1373 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.06433279133778247 |
[175] |
[149,81,172,95] |
0 |
hSpCas9 |
negative selection |
7979883 |
71120111 |
71120134 |
X |
- |
27260156 |
NCIH1373 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.6783222987500792 |
[517] |
[755,252,327,45] |
-6 |
hSpCas9 |
negative selection |
8044139 |
71120087 |
71120110 |
X |
- |
27260156 |
NCIH1373 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.1885975413348666 |
[244] |
[109,88,80,54] |
-8 |
hSpCas9 |
negative selection |
8044140 |
71119456 |
71119479 |
X |
+ |
27260156 |
NCIH1373 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.2535756364042906 |
[890] |
[756,496,1203,238] |
-3 |
hSpCas9 |
negative selection |
8044141 |
71119449 |
71119472 |
X |
- |
27260156 |
PATU8902 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-1.7233211223055243 |
[1672] |
[364,1022,569,925] |
-8 |
hSpCas9 |
negative selection |
8101132 |
71120989 |
71121012 |
X |
- |
27260156 |
PATU8902 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.6552533322571952 |
[600] |
[801,177,68,26] |
-8 |
hSpCas9 |
negative selection |
8101133 |
71121113 |
71121136 |
X |
+ |
27260156 |
PATU8902 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.3651270533284465 |
[175] |
[338,390,223,331] |
4 |
hSpCas9 |
negative selection |
8101134 |
71120111 |
71120134 |
X |
- |
27260156 |
PATU8902 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-1.219549916346712 |
[517] |
[194,437,315,284] |
-8 |
hSpCas9 |
negative selection |
8165390 |
71120087 |
71120110 |
X |
- |
27260156 |
PATU8902 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.5969722489266767 |
[244] |
[86,308,276,214] |
-5 |
hSpCas9 |
negative selection |
8165391 |
71119456 |
71119479 |
X |
+ |
27260156 |
PATU8902 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.7112640462944535 |
[890] |
[1009,870,420,814] |
-6 |
hSpCas9 |
negative selection |
8165392 |
71119449 |
71119472 |
X |
- |
27260156 |
PANC1 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.8957448234108953 |
[1672] |
[2553,3391,2220,2634] |
9 |
hSpCas9 |
negative selection |
8222383 |
71120989 |
71121012 |
X |
- |
27260156 |
PANC1 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
1.1250721715591248 |
[600] |
[1133,1200,911,1232] |
9 |
hSpCas9 |
negative selection |
8222384 |
71121113 |
71121136 |
X |
+ |
27260156 |
PANC1 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.11673284901504921 |
[175] |
[149,235,159,127] |
1 |
hSpCas9 |
negative selection |
8222385 |
71120111 |
71120134 |
X |
- |
27260156 |
PANC1 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
0.5306661018004308 |
[517] |
[470,819,861,476] |
8 |
hSpCas9 |
negative selection |
8286641 |
71120087 |
71120110 |
X |
- |
27260156 |
PANC1 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.22802313347895165 |
[244] |
[239,237,280,224] |
3 |
hSpCas9 |
negative selection |
8286642 |
71119456 |
71119479 |
X |
+ |
27260156 |
PANC1 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
1.239586840288644 |
[890] |
[1383,2013,2233,1647] |
9 |
hSpCas9 |
negative selection |
8286643 |
71119449 |
71119472 |
X |
- |
27260156 |
PANC0813 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.3613672108966337 |
[1672] |
[1970,1289,1475,1425] |
-5 |
hSpCas9 |
negative selection |
8343634 |
71120989 |
71121012 |
X |
- |
27260156 |
PANC0813 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.6046553086476067 |
[600] |
[498,446,321,583] |
-7 |
hSpCas9 |
negative selection |
8343635 |
71121113 |
71121136 |
X |
+ |
27260156 |
PANC0813 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.008636425036383955 |
[175] |
[154,367,128,175] |
0 |
hSpCas9 |
negative selection |
8343636 |
71120111 |
71120134 |
X |
- |
27260156 |
PANC0813 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.6022294456758098 |
[517] |
[410,482,358,352] |
-7 |
hSpCas9 |
negative selection |
8407892 |
71120087 |
71120110 |
X |
- |
27260156 |
PANC0813 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.15744393186689254 |
[244] |
[238,223,356,212] |
-3 |
hSpCas9 |
negative selection |
8407893 |
71119456 |
71119479 |
X |
+ |
27260156 |
PANC0813 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.030144390260784637 |
[890] |
[1522,1011,786,831] |
0 |
hSpCas9 |
negative selection |
8407894 |
71119449 |
71119472 |
X |
- |
27260156 |
RDES |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.4400513113663924 |
[1672] |
[1157,1401,1735,1399] |
-6 |
hSpCas9 |
negative selection |
8464885 |
71120989 |
71121012 |
X |
- |
27260156 |
RDES |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.9806473426452142 |
[600] |
[320,242,456,396] |
-9 |
hSpCas9 |
negative selection |
8464886 |
71121113 |
71121136 |
X |
+ |
27260156 |
RDES |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.016056226676620877 |
[175] |
[180,232,267,99] |
0 |
hSpCas9 |
negative selection |
8464887 |
71120111 |
71120134 |
X |
- |
27260156 |
RDES |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.20232979111779453 |
[517] |
[379,548,604,557] |
-3 |
hSpCas9 |
negative selection |
8529143 |
71120087 |
71120110 |
X |
- |
27260156 |
RDES |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.04727858397863749 |
[244] |
[347,242,230,326] |
0 |
hSpCas9 |
negative selection |
8529144 |
71119456 |
71119479 |
X |
+ |
27260156 |
RDES |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.015578695214250371 |
[890] |
[951,902,1045,1276] |
0 |
hSpCas9 |
negative selection |
8529145 |
71119449 |
71119472 |
X |
- |
27260156 |
PC3 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.03249606421775164 |
[1672] |
[973,1622,2738,1758] |
0 |
hSpCas9 |
negative selection |
8586136 |
71120989 |
71121012 |
X |
- |
27260156 |
PC3 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.3766902929048265 |
[600] |
[451,405,609,370] |
-7 |
hSpCas9 |
negative selection |
8586137 |
71121113 |
71121136 |
X |
+ |
27260156 |
PC3 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.09891181930299986 |
[175] |
[77,133,329,206] |
-2 |
hSpCas9 |
negative selection |
8586138 |
71120111 |
71120134 |
X |
- |
27260156 |
PC3 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.3813844040360844 |
[517] |
[293,444,459,407] |
-7 |
hSpCas9 |
negative selection |
8650394 |
71120087 |
71120110 |
X |
- |
27260156 |
PC3 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.04117395744261643 |
[244] |
[154,198,237,377] |
-1 |
hSpCas9 |
negative selection |
8650395 |
71119456 |
71119479 |
X |
+ |
27260156 |
PC3 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.154381903796584 |
[890] |
[588,818,1173,753] |
-3 |
hSpCas9 |
negative selection |
8650396 |
71119449 |
71119472 |
X |
- |
27260156 |
PATU8988T |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.4303113299275403 |
[1672] |
[1195,1204,1335,1047] |
-6 |
hSpCas9 |
negative selection |
8707387 |
71120989 |
71121012 |
X |
- |
27260156 |
PATU8988T |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.4954474933555908 |
[600] |
[190,230,171,234] |
-9 |
hSpCas9 |
negative selection |
8707388 |
71121113 |
71121136 |
X |
+ |
27260156 |
PATU8988T |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.006039206701922373 |
[175] |
[26,111,363,171] |
0 |
hSpCas9 |
negative selection |
8707389 |
71120111 |
71120134 |
X |
- |
27260156 |
PATU8988T |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.4302762952941578 |
[517] |
[387,282,498,299] |
-6 |
hSpCas9 |
negative selection |
8771645 |
71120087 |
71120110 |
X |
- |
27260156 |
PATU8988T |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.12984299182624626 |
[244] |
[489,249,149,136] |
2 |
hSpCas9 |
negative selection |
8771646 |
71119456 |
71119479 |
X |
+ |
27260156 |
PATU8988T |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.5091413559266684 |
[890] |
[737,686,558,429] |
-7 |
hSpCas9 |
negative selection |
8771647 |
71119449 |
71119472 |
X |
- |
27260156 |
T47D |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.36395341298444017 |
[1672] |
[1516,1411,1550,1587] |
-7 |
hSpCas9 |
negative selection |
8828638 |
71120989 |
71121012 |
X |
- |
27260156 |
T47D |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.7358110157894043 |
[600] |
[406,381,413,483] |
-9 |
hSpCas9 |
negative selection |
8828639 |
71121113 |
71121136 |
X |
+ |
27260156 |
T47D |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.14068695138503995 |
[175] |
[156,155,254,176] |
-3 |
hSpCas9 |
negative selection |
8828640 |
71120111 |
71120134 |
X |
- |
27260156 |
T47D |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.14714641306267684 |
[517] |
[667,445,549,523] |
-3 |
hSpCas9 |
negative selection |
8892896 |
71120087 |
71120110 |
X |
- |
27260156 |
T47D |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.08325460107301841 |
[244] |
[253,272,280,268] |
-2 |
hSpCas9 |
negative selection |
8892897 |
71119456 |
71119479 |
X |
+ |
27260156 |
T47D |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.32175581573504464 |
[890] |
[981,657,801,897] |
-6 |
hSpCas9 |
negative selection |
8892898 |
71119449 |
71119472 |
X |
- |
27260156 |
SU8686 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.697807870042437 |
[1672] |
[1017,937,1079,1066] |
-8 |
hSpCas9 |
negative selection |
8949889 |
71120989 |
71121012 |
X |
- |
27260156 |
SU8686 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.8306245083911887 |
[600] |
[164,225,79,191] |
-9 |
hSpCas9 |
negative selection |
8949890 |
71121113 |
71121136 |
X |
+ |
27260156 |
SU8686 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.5041011548940089 |
[175] |
[71,164,111,145] |
-7 |
hSpCas9 |
negative selection |
8949891 |
71120111 |
71120134 |
X |
- |
27260156 |
SU8686 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.598688720532597 |
[517] |
[289,225,247,659] |
-7 |
hSpCas9 |
negative selection |
9014147 |
71120087 |
71120110 |
X |
- |
27260156 |
SU8686 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.6938733030125519 |
[244] |
[108,108,176,227] |
-7 |
hSpCas9 |
negative selection |
9014148 |
71119456 |
71119479 |
X |
+ |
27260156 |
SU8686 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.6855433199132757 |
[890] |
[519,487,624,577] |
-7 |
hSpCas9 |
negative selection |
9014149 |
71119449 |
71119472 |
X |
- |
27260156 |
SKES1 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.5206360693758854 |
[1672] |
[1309,1333,1121,942] |
-8 |
hSpCas9 |
negative selection |
9071140 |
71120989 |
71121012 |
X |
- |
27260156 |
SKES1 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.6746872693631717 |
[600] |
[419,370,478,247] |
-9 |
hSpCas9 |
negative selection |
9071141 |
71121113 |
71121136 |
X |
+ |
27260156 |
SKES1 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.2229549710547627 |
[175] |
[366,173,156,145] |
5 |
hSpCas9 |
negative selection |
9071142 |
71120111 |
71120134 |
X |
- |
27260156 |
SKES1 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.378056078464885 |
[517] |
[494,457,311,348] |
-7 |
hSpCas9 |
negative selection |
9135398 |
71120087 |
71120110 |
X |
- |
27260156 |
SKES1 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.27815583826448864 |
[244] |
[100,263,155,268] |
-6 |
hSpCas9 |
negative selection |
9135399 |
71119456 |
71119479 |
X |
+ |
27260156 |
SKES1 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.29378619137901285 |
[890] |
[773,746,793,600] |
-6 |
hSpCas9 |
negative selection |
9135400 |
71119449 |
71119472 |
X |
- |
27260156 |
TOV112D |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.14621512872139975 |
[1672] |
[2037,2025,1846,1568] |
3 |
hSpCas9 |
negative selection |
9192391 |
71120989 |
71121012 |
X |
- |
27260156 |
TOV112D |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.2912734656818096 |
[600] |
[632,481,543,321] |
-5 |
hSpCas9 |
negative selection |
9192392 |
71121113 |
71121136 |
X |
+ |
27260156 |
TOV112D |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.34329317771233314 |
[175] |
[132,97,175,137] |
-6 |
hSpCas9 |
negative selection |
9192393 |
71120111 |
71120134 |
X |
- |
27260156 |
TOV112D |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
0.01292815776322176 |
[517] |
[389,715,674,352] |
0 |
hSpCas9 |
negative selection |
9256649 |
71120087 |
71120110 |
X |
- |
27260156 |
TOV112D |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.10678795907821459 |
[244] |
[261,284,198,313] |
2 |
hSpCas9 |
negative selection |
9256650 |
71119456 |
71119479 |
X |
+ |
27260156 |
TOV112D |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.21666203766322734 |
[890] |
[1168,984,788,1196] |
4 |
hSpCas9 |
negative selection |
9256651 |
71119449 |
71119472 |
X |
- |
27260156 |
TC71 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
0.07635777501670926 |
[1672] |
[1808,2033,1801,1924] |
2 |
hSpCas9 |
negative selection |
9313642 |
71120989 |
71121012 |
X |
- |
27260156 |
TC71 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-0.2763922109330412 |
[600] |
[519,520,505,584] |
-6 |
hSpCas9 |
negative selection |
9313643 |
71121113 |
71121136 |
X |
+ |
27260156 |
TC71 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
-0.1169699156209083 |
[175] |
[182,183,157,170] |
-3 |
hSpCas9 |
negative selection |
9313644 |
71120111 |
71120134 |
X |
- |
27260156 |
TC71 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.2171839159825949 |
[517] |
[439,523,476,469] |
-5 |
hSpCas9 |
negative selection |
9377900 |
71120087 |
71120110 |
X |
- |
27260156 |
TC71 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.21747087202346416 |
[244] |
[195,238,198,273] |
-5 |
hSpCas9 |
negative selection |
9377901 |
71119456 |
71119479 |
X |
+ |
27260156 |
TC71 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
0.1684594166178135 |
[890] |
[874,897,1179,1358] |
4 |
hSpCas9 |
negative selection |
9377902 |
71119449 |
71119472 |
X |
- |
27260156 |
TC32 |
viability |
AGGATTGAAGCTGACGTTCTTGG |
MED12 |
ENSG00000184634 |
-0.5340849986550369 |
[1672] |
[1025,738,1714,1045] |
-8 |
hSpCas9 |
negative selection |
9434893 |
71120989 |
71121012 |
X |
- |
27260156 |
TC32 |
viability |
TAACTGCTCCCATAAGTACTTGG |
MED12 |
ENSG00000184634 |
-1.0122370016382631 |
[600] |
[268,101,429,406] |
-9 |
hSpCas9 |
negative selection |
9434894 |
71121113 |
71121136 |
X |
+ |
27260156 |
TC32 |
viability |
GTGGGATTACACCGAGAAGCTGG |
MED12 |
ENSG00000184634 |
0.02664875185611959 |
[175] |
[119,117,218,245] |
0 |
hSpCas9 |
negative selection |
9434895 |
71120111 |
71120134 |
X |
- |
27260156 |
TC32 |
viability |
CTCAGAGATTGCTGCATAGTAGG |
MED12 |
ENSG00000184634 |
-0.20214467278867948 |
[517] |
[390,364,426,514] |
-4 |
hSpCas9 |
negative selection |
9499151 |
71120087 |
71120110 |
X |
- |
27260156 |
TC32 |
viability |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.2213746913167618 |
[244] |
[172,109,167,368] |
-4 |
hSpCas9 |
negative selection |
9499152 |
71119456 |
71119479 |
X |
+ |
27260156 |
TC32 |
viability |
CGTCAGCTTCAATCCTGCCAAGG |
MED12 |
ENSG00000184634 |
-0.3350282338584839 |
[890] |
[630,462,905,742] |
-6 |
hSpCas9 |
negative selection |
9499153 |
71118815 |
71118838 |
X |
- |
27869803 |
HPAFII |
viability after 27 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-1.3445725960690134 |
[201] |
[31,49,NaN] |
-7 |
hSpCas9 |
negative selection |
9609491 |
71119735 |
71119758 |
X |
- |
27869803 |
HPAFII |
viability after 27 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.0568556490340715 |
[812] |
[87,114,NaN] |
-8 |
hSpCas9 |
negative selection |
9609492 |
71120087 |
71120110 |
X |
- |
27869803 |
HPAFII |
viability after 27 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.07241954562429642 |
[123] |
[115,16,NaN] |
0 |
hSpCas9 |
negative selection |
9609493 |
71121019 |
71121042 |
X |
+ |
27869803 |
HPAFII |
viability after 27 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.0800621330103766 |
[273] |
[345,269,NaN] |
8 |
hSpCas9 |
negative selection |
9609494 |
71121386 |
71121409 |
X |
- |
27869803 |
HPAFII |
viability after 27 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-4.420819851872849 |
[299] |
[8,5,NaN] |
-9 |
hSpCas9 |
negative selection |
9609495 |
71121596 |
71121619 |
X |
- |
27869803 |
HPAFII |
viability after 27 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-5.531851164261594 |
[127] |
[1,0,NaN] |
-9 |
hSpCas9 |
negative selection |
9609496 |
71118815 |
71118838 |
X |
- |
27869803 |
HPAFII |
viability after 15 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-1.0299673930886237 |
[201] |
[101,108,NaN] |
-8 |
hSpCas9 |
negative selection |
9691940 |
71119735 |
71119758 |
X |
- |
27869803 |
HPAFII |
viability after 15 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-1.5394321126599826 |
[812] |
[196,364,NaN] |
-8 |
hSpCas9 |
negative selection |
9691941 |
71120087 |
71120110 |
X |
- |
27869803 |
HPAFII |
viability after 15 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.4809019172663349 |
[123] |
[158,55,NaN] |
-5 |
hSpCas9 |
negative selection |
9691942 |
71121019 |
71121042 |
X |
+ |
27869803 |
HPAFII |
viability after 15 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
1.1373439906187455 |
[273] |
[915,480,NaN] |
9 |
hSpCas9 |
negative selection |
9691943 |
71121386 |
71121409 |
X |
- |
27869803 |
HPAFII |
viability after 15 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-2.22426851747188 |
[299] |
[68,68,NaN] |
-9 |
hSpCas9 |
negative selection |
9691944 |
71121596 |
71121619 |
X |
- |
27869803 |
HPAFII |
viability after 15 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-7.103974283754168 |
[127] |
[0,0,NaN] |
-9 |
hSpCas9 |
negative selection |
9691945 |
71118815 |
71118838 |
X |
- |
27869803 |
ASPC1 |
viability after 36 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-1.2076758028642918 |
[289] |
[42,73,19] |
-8 |
hSpCas9 |
negative selection |
9774389 |
71119735 |
71119758 |
X |
- |
27869803 |
ASPC1 |
viability after 36 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-1.4754754583504373 |
[1878] |
[356,248,137] |
-8 |
hSpCas9 |
negative selection |
9774390 |
71120087 |
71120110 |
X |
- |
27869803 |
ASPC1 |
viability after 36 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
0.46940766523070865 |
[324] |
[285,20,172] |
5 |
hSpCas9 |
negative selection |
9774391 |
71121019 |
71121042 |
X |
+ |
27869803 |
ASPC1 |
viability after 36 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.5313739573591759 |
[555] |
[410,112,318] |
5 |
hSpCas9 |
negative selection |
9774392 |
71121386 |
71121409 |
X |
- |
27869803 |
ASPC1 |
viability after 36 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-0.6015023825023731 |
[852] |
[124,300,160] |
-5 |
hSpCas9 |
negative selection |
9774393 |
71121596 |
71121619 |
X |
- |
27869803 |
ASPC1 |
viability after 36 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-2.643551008431436 |
[419] |
[0,64,5] |
-9 |
hSpCas9 |
negative selection |
9774394 |
71118815 |
71118838 |
X |
- |
27869803 |
PATU8988S |
viability after 35 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-2.8673722596580364 |
[344] |
[36,0,NaN] |
-9 |
hSpCas9 |
negative selection |
9856838 |
71119735 |
71119758 |
X |
- |
27869803 |
PATU8988S |
viability after 35 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-4.168327110244336 |
[1831] |
[56,24,NaN] |
-9 |
hSpCas9 |
negative selection |
9856839 |
71120087 |
71120110 |
X |
- |
27869803 |
PATU8988S |
viability after 35 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.0367416869415658 |
[320] |
[69,55,NaN] |
-7 |
hSpCas9 |
negative selection |
9856840 |
71121019 |
71121042 |
X |
+ |
27869803 |
PATU8988S |
viability after 35 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
-0.5092722499297083 |
[742] |
[96,323,NaN] |
-5 |
hSpCas9 |
negative selection |
9856841 |
71121386 |
71121409 |
X |
- |
27869803 |
PATU8988S |
viability after 35 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-3.327937877509608 |
[773] |
[49,11,NaN] |
-9 |
hSpCas9 |
negative selection |
9856842 |
71121596 |
71121619 |
X |
- |
27869803 |
PATU8988S |
viability after 35 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-3.1286431411863775 |
[347] |
[26,4,NaN] |
-9 |
hSpCas9 |
negative selection |
9856843 |
71118815 |
71118838 |
X |
- |
27869803 |
PATU8988S |
viability after 31 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-3.3682470694333237 |
[344] |
[22,0,NaN] |
-9 |
hSpCas9 |
negative selection |
9939287 |
71119735 |
71119758 |
X |
- |
27869803 |
PATU8988S |
viability after 31 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-3.551907193927618 |
[1831] |
[89,26,NaN] |
-9 |
hSpCas9 |
negative selection |
9939288 |
71120087 |
71120110 |
X |
- |
27869803 |
PATU8988S |
viability after 31 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-0.9040091793159493 |
[320] |
[74,59,NaN] |
-7 |
hSpCas9 |
negative selection |
9939289 |
71121019 |
71121042 |
X |
+ |
27869803 |
PATU8988S |
viability after 31 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
-0.4812576287035663 |
[742] |
[169,265,NaN] |
-5 |
hSpCas9 |
negative selection |
9939290 |
71121386 |
71121409 |
X |
- |
27869803 |
PATU8988S |
viability after 31 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-2.839279495429099 |
[773] |
[65,13,NaN] |
-9 |
hSpCas9 |
negative selection |
9939291 |
71121596 |
71121619 |
X |
- |
27869803 |
PATU8988S |
viability after 31 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-2.264373256924736 |
[347] |
[38,15,NaN] |
-9 |
hSpCas9 |
negative selection |
9939292 |
71118815 |
71118838 |
X |
- |
27869803 |
HPAFII |
viability after 35 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-2.4061554680557453 |
[201] |
[15,22,NaN] |
-8 |
hSpCas9 |
negative selection |
10021736 |
71119735 |
71119758 |
X |
- |
27869803 |
HPAFII |
viability after 35 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.171100387429534 |
[812] |
[41,146,NaN] |
-8 |
hSpCas9 |
negative selection |
10021737 |
71120087 |
71120110 |
X |
- |
27869803 |
HPAFII |
viability after 35 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.5473024818625352 |
[123] |
[36,3,NaN] |
-7 |
hSpCas9 |
negative selection |
10021738 |
71121019 |
71121042 |
X |
+ |
27869803 |
HPAFII |
viability after 35 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.8404125383369043 |
[273] |
[285,205,NaN] |
5 |
hSpCas9 |
negative selection |
10021739 |
71121386 |
71121409 |
X |
- |
27869803 |
HPAFII |
viability after 35 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-3.4698355289716813 |
[299] |
[16,9,NaN] |
-9 |
hSpCas9 |
negative selection |
10021740 |
71121596 |
71121619 |
X |
- |
27869803 |
HPAFII |
viability after 35 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-6.017911447003325 |
[127] |
[0,0,NaN] |
-9 |
hSpCas9 |
negative selection |
10021741 |
71118815 |
71118838 |
X |
- |
27869803 |
HPAFII |
viability after 31 days |
TCCTGAGGGTAAACATCGGGAGG |
MED12 |
ENSG00000184634 |
-1.0878102843193116 |
[201] |
[71,32,NaN] |
-6 |
hSpCas9 |
negative selection |
10104185 |
71119735 |
71119758 |
X |
- |
27869803 |
HPAFII |
viability after 31 days |
CCTGCGACCAGTGTCAGGAAGGG |
MED12 |
ENSG00000184634 |
-2.116651495383129 |
[812] |
[53,160,NaN] |
-8 |
hSpCas9 |
negative selection |
10104186 |
71120087 |
71120110 |
X |
- |
27869803 |
HPAFII |
viability after 31 days |
ACAGGTCATCTTAATGAGCCAGG |
MED12 |
ENSG00000184634 |
-1.403834216306677 |
[123] |
[32,18,NaN] |
-7 |
hSpCas9 |
negative selection |
10104187 |
71121019 |
71121042 |
X |
+ |
27869803 |
HPAFII |
viability after 31 days |
TGGCTGAATACTACCGGCCAGGG |
MED12 |
ENSG00000184634 |
0.43379574857672154 |
[273] |
[178,238,NaN] |
3 |
hSpCas9 |
negative selection |
10104188 |
71121386 |
71121409 |
X |
- |
27869803 |
HPAFII |
viability after 31 days |
GCAATTCATCCTCTCCAGGGCGG |
MED12 |
ENSG00000184634 |
-3.1111025787414173 |
[299] |
[7,31,NaN] |
-9 |
hSpCas9 |
negative selection |
10104189 |
71121596 |
71121619 |
X |
- |
27869803 |
HPAFII |
viability after 31 days |
ACAGAAGTAGGCAAGCCGGCGGG |
MED12 |
ENSG00000184634 |
-6.166628800324743 |
[127] |
[0,0,NaN] |
-9 |
hSpCas9 |
negative selection |
10104190 |
71120160 |
71120183 |
X |
- |
28162770 |
P31FUJ |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.711970041112938 |
[183] |
[32] |
-9 |
hSpCas9 |
negative selection |
10190597 |
71126379 |
71126402 |
X |
- |
28162770 |
P31FUJ |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-4.810675280349216 |
[405] |
[16] |
-9 |
hSpCas9 |
negative selection |
10190598 |
71125361 |
71125384 |
X |
+ |
28162770 |
P31FUJ |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-4.741815851902237 |
[295] |
[12] |
-9 |
hSpCas9 |
negative selection |
10190599 |
71132900 |
71132923 |
X |
+ |
28162770 |
P31FUJ |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-1.9376741688707315 |
[162] |
[49] |
-8 |
hSpCas9 |
negative selection |
10190600 |
71134388 |
71134411 |
X |
+ |
28162770 |
P31FUJ |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-1.3674517311091605 |
[100] |
[45] |
-7 |
hSpCas9 |
negative selection |
10190601 |
71119757 |
71119780 |
X |
+ |
28162770 |
P31FUJ |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.2068069958814343 |
[164] |
[83] |
-7 |
hSpCas9 |
negative selection |
10190602 |
71123631 |
71123654 |
X |
- |
28162770 |
P31FUJ |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.4027272058566909 |
[53] |
[23] |
-7 |
hSpCas9 |
negative selection |
10190603 |
71124305 |
71124328 |
X |
- |
28162770 |
P31FUJ |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.3862121448412299 |
[320] |
[492] |
4 |
hSpCas9 |
negative selection |
10190604 |
71125083 |
71125106 |
X |
- |
28162770 |
P31FUJ |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-3.1346218104754753 |
[283] |
[37] |
-9 |
hSpCas9 |
negative selection |
10190605 |
71125377 |
71125400 |
X |
- |
28162770 |
P31FUJ |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-6.320265045664717 |
[67] |
[0] |
-9 |
hSpCas9 |
negative selection |
10190606 |
71120160 |
71120183 |
X |
- |
28162770 |
TF1 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[19] |
1 |
hSpCas9 |
negative selection |
10359963 |
71126379 |
71126402 |
X |
- |
28162770 |
TF1 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[35] |
1 |
hSpCas9 |
negative selection |
10359964 |
71125361 |
71125384 |
X |
+ |
28162770 |
TF1 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[2] |
1 |
hSpCas9 |
negative selection |
10359965 |
71132900 |
71132923 |
X |
+ |
28162770 |
TF1 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[43] |
1 |
hSpCas9 |
negative selection |
10359966 |
71134388 |
71134411 |
X |
+ |
28162770 |
TF1 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[0] |
1 |
hSpCas9 |
negative selection |
10359967 |
71119757 |
71119780 |
X |
+ |
28162770 |
TF1 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[91] |
1 |
hSpCas9 |
negative selection |
10359968 |
71123631 |
71123654 |
X |
- |
28162770 |
TF1 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[12] |
1 |
hSpCas9 |
negative selection |
10359969 |
71124305 |
71124328 |
X |
- |
28162770 |
TF1 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[284] |
1 |
hSpCas9 |
negative selection |
10359970 |
71125083 |
71125106 |
X |
- |
28162770 |
TF1 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[122] |
1 |
hSpCas9 |
negative selection |
10359971 |
71125377 |
71125400 |
X |
- |
28162770 |
TF1 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
NaN |
[NaN] |
[0] |
1 |
hSpCas9 |
negative selection |
10359972 |
71120160 |
71120183 |
X |
- |
28162770 |
SKM1 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.796006489489061 |
[54] |
[13] |
-9 |
hSpCas9 |
negative selection |
10529329 |
71126379 |
71126402 |
X |
- |
28162770 |
SKM1 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.178936242737281 |
[72] |
[56] |
-7 |
hSpCas9 |
negative selection |
10529330 |
71125361 |
71125384 |
X |
+ |
28162770 |
SKM1 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-4.669998604576956 |
[71] |
[4] |
-9 |
hSpCas9 |
negative selection |
10529331 |
71132900 |
71132923 |
X |
+ |
28162770 |
SKM1 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-2.7548875021634687 |
[41] |
[10] |
-9 |
hSpCas9 |
negative selection |
10529332 |
71134388 |
71134411 |
X |
+ |
28162770 |
SKM1 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-0.3931583992181311 |
[25] |
[34] |
-3 |
hSpCas9 |
negative selection |
10529333 |
71119757 |
71119780 |
X |
+ |
28162770 |
SKM1 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-0.19751083311421172 |
[47] |
[73] |
-2 |
hSpCas9 |
negative selection |
10529334 |
71123631 |
71123654 |
X |
- |
28162770 |
SKM1 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-0.2370391973008492 |
[19] |
[29] |
-2 |
hSpCas9 |
negative selection |
10529335 |
71124305 |
71124328 |
X |
- |
28162770 |
SKM1 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.2681961109495726 |
[61] |
[131] |
2 |
hSpCas9 |
negative selection |
10529336 |
71125083 |
71125106 |
X |
- |
28162770 |
SKM1 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
0.7904415391212576 |
[51] |
[158] |
7 |
hSpCas9 |
negative selection |
10529337 |
71125377 |
71125400 |
X |
- |
28162770 |
SKM1 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-1.9094645392723446 |
[16] |
[7] |
-8 |
hSpCas9 |
negative selection |
10529338 |
71120160 |
71120183 |
X |
- |
28162770 |
SKM1 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.796006489489061 |
[54] |
[13] |
-9 |
hSpCas9 |
negative selection |
10698695 |
71126379 |
71126402 |
X |
- |
28162770 |
SKM1 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.178936242737281 |
[72] |
[56] |
-7 |
hSpCas9 |
negative selection |
10698696 |
71125361 |
71125384 |
X |
+ |
28162770 |
SKM1 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-4.669998604576956 |
[71] |
[4] |
-9 |
hSpCas9 |
negative selection |
10698697 |
71132900 |
71132923 |
X |
+ |
28162770 |
SKM1 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-2.7548875021634687 |
[41] |
[10] |
-9 |
hSpCas9 |
negative selection |
10698698 |
71134388 |
71134411 |
X |
+ |
28162770 |
SKM1 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-0.3931583992181311 |
[25] |
[34] |
-3 |
hSpCas9 |
negative selection |
10698699 |
71119757 |
71119780 |
X |
+ |
28162770 |
SKM1 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-0.19751083311421172 |
[47] |
[73] |
-2 |
hSpCas9 |
negative selection |
10698700 |
71123631 |
71123654 |
X |
- |
28162770 |
SKM1 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-0.2370391973008492 |
[19] |
[29] |
-2 |
hSpCas9 |
negative selection |
10698701 |
71124305 |
71124328 |
X |
- |
28162770 |
SKM1 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.2681961109495726 |
[61] |
[131] |
2 |
hSpCas9 |
negative selection |
10698702 |
71125083 |
71125106 |
X |
- |
28162770 |
SKM1 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
0.7904415391212576 |
[51] |
[158] |
7 |
hSpCas9 |
negative selection |
10698703 |
71125377 |
71125400 |
X |
- |
28162770 |
SKM1 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-1.9094645392723446 |
[16] |
[7] |
-8 |
hSpCas9 |
negative selection |
10698704 |
71120160 |
71120183 |
X |
- |
28162770 |
PL21 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.017091101731349 |
[185] |
[19] |
-8 |
hSpCas9 |
negative selection |
10868061 |
71126379 |
71126402 |
X |
- |
28162770 |
PL21 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.070507975454349 |
[303] |
[62] |
-6 |
hSpCas9 |
negative selection |
10868062 |
71125361 |
71125384 |
X |
+ |
28162770 |
PL21 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-3.314433558340438 |
[319] |
[13] |
-9 |
hSpCas9 |
negative selection |
10868063 |
71132900 |
71132923 |
X |
+ |
28162770 |
PL21 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-1.789806720846757 |
[142] |
[17] |
-8 |
hSpCas9 |
negative selection |
10868064 |
71134388 |
71134411 |
X |
+ |
28162770 |
PL21 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-0.47793229062331744 |
[79] |
[24] |
-3 |
hSpCas9 |
negative selection |
10868065 |
71119757 |
71119780 |
X |
+ |
28162770 |
PL21 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-3.6661089966218525 |
[174] |
[5] |
-9 |
hSpCas9 |
negative selection |
10868066 |
71123631 |
71123654 |
X |
- |
28162770 |
PL21 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.5547478876741483 |
[53] |
[7] |
-7 |
hSpCas9 |
negative selection |
10868067 |
71124305 |
71124328 |
X |
- |
28162770 |
PL21 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.10821712504828093 |
[161] |
[75] |
1 |
hSpCas9 |
negative selection |
10868068 |
71125083 |
71125106 |
X |
- |
28162770 |
PL21 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-1.915337602930616 |
[155] |
[17] |
-8 |
hSpCas9 |
negative selection |
10868069 |
71125377 |
71125400 |
X |
- |
28162770 |
PL21 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-4.085262604372929 |
[38] |
[0] |
-9 |
hSpCas9 |
negative selection |
10868070 |
71120160 |
71120183 |
X |
- |
28162770 |
P31FUJ |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.711970041112938 |
[183] |
[32] |
-9 |
hSpCas9 |
negative selection |
11037427 |
71126379 |
71126402 |
X |
- |
28162770 |
P31FUJ |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-4.810675280349216 |
[405] |
[16] |
-9 |
hSpCas9 |
negative selection |
11037428 |
71125361 |
71125384 |
X |
+ |
28162770 |
P31FUJ |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-4.741815851902237 |
[295] |
[12] |
-9 |
hSpCas9 |
negative selection |
11037429 |
71132900 |
71132923 |
X |
+ |
28162770 |
P31FUJ |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-1.9376741688707315 |
[162] |
[49] |
-8 |
hSpCas9 |
negative selection |
11037430 |
71134388 |
71134411 |
X |
+ |
28162770 |
P31FUJ |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-1.3674517311091605 |
[100] |
[45] |
-7 |
hSpCas9 |
negative selection |
11037431 |
71119757 |
71119780 |
X |
+ |
28162770 |
P31FUJ |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.2068069958814343 |
[164] |
[83] |
-7 |
hSpCas9 |
negative selection |
11037432 |
71123631 |
71123654 |
X |
- |
28162770 |
P31FUJ |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.4027272058566909 |
[53] |
[23] |
-7 |
hSpCas9 |
negative selection |
11037433 |
71124305 |
71124328 |
X |
- |
28162770 |
P31FUJ |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.3862121448412299 |
[320] |
[492] |
4 |
hSpCas9 |
negative selection |
11037434 |
71125083 |
71125106 |
X |
- |
28162770 |
P31FUJ |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-3.1346218104754753 |
[283] |
[37] |
-9 |
hSpCas9 |
negative selection |
11037435 |
71125377 |
71125400 |
X |
- |
28162770 |
P31FUJ |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-6.320265045664717 |
[67] |
[0] |
-9 |
hSpCas9 |
negative selection |
11037436 |
71120160 |
71120183 |
X |
- |
28162770 |
OCIAML5 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-6.437029071585154 |
[95] |
[1] |
-9 |
hSpCas9 |
negative selection |
11206793 |
71126379 |
71126402 |
X |
- |
28162770 |
OCIAML5 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.9740570952426075 |
[184] |
[84] |
-8 |
hSpCas9 |
negative selection |
11206794 |
71125361 |
71125384 |
X |
+ |
28162770 |
OCIAML5 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-4.008571056543988 |
[106] |
[11] |
-9 |
hSpCas9 |
negative selection |
11206795 |
71132900 |
71132923 |
X |
+ |
28162770 |
OCIAML5 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-4.365136153103368 |
[136] |
[11] |
-9 |
hSpCas9 |
negative selection |
11206796 |
71134388 |
71134411 |
X |
+ |
28162770 |
OCIAML5 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-0.13122064206106798 |
[53] |
[88] |
-1 |
hSpCas9 |
negative selection |
11206797 |
71119757 |
71119780 |
X |
+ |
28162770 |
OCIAML5 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.869553997592838 |
[82] |
[40] |
-7 |
hSpCas9 |
negative selection |
11206798 |
71123631 |
71123654 |
X |
- |
28162770 |
OCIAML5 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-3.5301384759766345 |
[63] |
[9] |
-9 |
hSpCas9 |
negative selection |
11206799 |
71124305 |
71124328 |
X |
- |
28162770 |
OCIAML5 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.5460971098504506 |
[128] |
[339] |
5 |
hSpCas9 |
negative selection |
11206800 |
71125083 |
71125106 |
X |
- |
28162770 |
OCIAML5 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-2.115100976697791 |
[179] |
[74] |
-8 |
hSpCas9 |
negative selection |
11206801 |
71125377 |
71125400 |
X |
- |
28162770 |
OCIAML5 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-4.137468789726245 |
[38] |
[3] |
-9 |
hSpCas9 |
negative selection |
11206802 |
71120160 |
71120183 |
X |
- |
28162770 |
EOL1 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.830339730592934 |
[296] |
[21] |
-9 |
hSpCas9 |
negative selection |
11376159 |
71126379 |
71126402 |
X |
- |
28162770 |
EOL1 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.0208169718526197 |
[284] |
[73] |
-6 |
hSpCas9 |
negative selection |
11376160 |
71125361 |
71125384 |
X |
+ |
28162770 |
EOL1 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-3.943348692422121 |
[583] |
[19] |
-9 |
hSpCas9 |
negative selection |
11376161 |
71132900 |
71132923 |
X |
+ |
28162770 |
EOL1 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-1.8480417323263931 |
[327] |
[47] |
-8 |
hSpCas9 |
negative selection |
11376162 |
71134388 |
71134411 |
X |
+ |
28162770 |
EOL1 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
0.5577654408989117 |
[97] |
[75] |
5 |
hSpCas9 |
negative selection |
11376163 |
71119757 |
71119780 |
X |
+ |
28162770 |
EOL1 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-2.576022541860249 |
[248] |
[21] |
-9 |
hSpCas9 |
negative selection |
11376164 |
71123631 |
71123654 |
X |
- |
28162770 |
EOL1 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-2.8409869747924423 |
[67] |
[4] |
-9 |
hSpCas9 |
negative selection |
11376165 |
71124305 |
71124328 |
X |
- |
28162770 |
EOL1 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
1.3582009490167253 |
[230] |
[311] |
9 |
hSpCas9 |
negative selection |
11376166 |
71125083 |
71125106 |
X |
- |
28162770 |
EOL1 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-1.419406629646827 |
[197] |
[38] |
-7 |
hSpCas9 |
negative selection |
11376167 |
71125377 |
71125400 |
X |
- |
28162770 |
EOL1 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-5.09782004145792 |
[64] |
[0] |
-9 |
hSpCas9 |
negative selection |
11376168 |
71120160 |
71120183 |
X |
- |
28162770 |
MOLM13 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-5.297645364818399 |
[271] |
[4] |
-9 |
hSpCas9 |
negative selection |
11545525 |
71126379 |
71126402 |
X |
- |
28162770 |
MOLM13 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-2.6121750073846 |
[388] |
[45] |
-8 |
hSpCas9 |
negative selection |
11545526 |
71125361 |
71125384 |
X |
+ |
28162770 |
MOLM13 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-6.320013177846853 |
[441] |
[3] |
-9 |
hSpCas9 |
negative selection |
11545527 |
71132900 |
71132923 |
X |
+ |
28162770 |
MOLM13 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-2.2954103604350897 |
[257] |
[37] |
-8 |
hSpCas9 |
negative selection |
11545528 |
71134388 |
71134411 |
X |
+ |
28162770 |
MOLM13 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-0.104016966351131 |
[109] |
[73] |
0 |
hSpCas9 |
negative selection |
11545529 |
71119757 |
71119780 |
X |
+ |
28162770 |
MOLM13 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-2.8879860452661212 |
[214] |
[20] |
-8 |
hSpCas9 |
negative selection |
11545530 |
71123631 |
71123654 |
X |
- |
28162770 |
MOLM13 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.483201017974475 |
[57] |
[14] |
-6 |
hSpCas9 |
negative selection |
11545531 |
71124305 |
71124328 |
X |
- |
28162770 |
MOLM13 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.8585302265159552 |
[327] |
[429] |
6 |
hSpCas9 |
negative selection |
11545532 |
71125083 |
71125106 |
X |
- |
28162770 |
MOLM13 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-0.8953655756317186 |
[300] |
[116] |
-5 |
hSpCas9 |
negative selection |
11545533 |
71125377 |
71125400 |
X |
- |
28162770 |
MOLM13 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-5.509390541955338 |
[62] |
[0] |
-9 |
hSpCas9 |
negative selection |
11545534 |
71120160 |
71120183 |
X |
- |
28162770 |
HEL |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-1.9761710006441369 |
[300] |
[48] |
-8 |
hSpCas9 |
negative selection |
11714891 |
71126379 |
71126402 |
X |
- |
28162770 |
HEL |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-0.864221156719526 |
[377] |
[132] |
-5 |
hSpCas9 |
negative selection |
11714892 |
71125361 |
71125384 |
X |
+ |
28162770 |
HEL |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-1.6033355083677514 |
[388] |
[81] |
-7 |
hSpCas9 |
negative selection |
11714893 |
71132900 |
71132923 |
X |
+ |
28162770 |
HEL |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-0.36884914227485466 |
[249] |
[123] |
-3 |
hSpCas9 |
negative selection |
11714894 |
71134388 |
71134411 |
X |
+ |
28162770 |
HEL |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-0.7602258349779119 |
[118] |
[44] |
-5 |
hSpCas9 |
negative selection |
11714895 |
71119757 |
71119780 |
X |
+ |
28162770 |
HEL |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.357261167999643 |
[211] |
[52] |
-7 |
hSpCas9 |
negative selection |
11714896 |
71123631 |
71123654 |
X |
- |
28162770 |
HEL |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-1.7357727912533731 |
[77] |
[14] |
-7 |
hSpCas9 |
negative selection |
11714897 |
71124305 |
71124328 |
X |
- |
28162770 |
HEL |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.22770133272151313 |
[267] |
[200] |
1 |
hSpCas9 |
negative selection |
11714898 |
71125083 |
71125106 |
X |
- |
28162770 |
HEL |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-0.3319500794704555 |
[225] |
[114] |
-2 |
hSpCas9 |
negative selection |
11714899 |
71125377 |
71125400 |
X |
- |
28162770 |
HEL |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-5.28799850556253 |
[60] |
[0] |
-9 |
hSpCas9 |
negative selection |
11714900 |
71120160 |
71120183 |
X |
- |
28162770 |
MV411 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-1.7732219197833177 |
[210] |
[51] |
-8 |
hSpCas9 |
negative selection |
11884257 |
71126379 |
71126402 |
X |
- |
28162770 |
MV411 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.2776534939609823 |
[235] |
[81] |
-7 |
hSpCas9 |
negative selection |
11884258 |
71125361 |
71125384 |
X |
+ |
28162770 |
MV411 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-2.136109662368253 |
[286] |
[54] |
-8 |
hSpCas9 |
negative selection |
11884259 |
71132900 |
71132923 |
X |
+ |
28162770 |
MV411 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-3.7615512324444795 |
[160] |
[9] |
-9 |
hSpCas9 |
negative selection |
11884260 |
71134388 |
71134411 |
X |
+ |
28162770 |
MV411 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-2.357424507376086 |
[72] |
[11] |
-8 |
hSpCas9 |
negative selection |
11884261 |
71119757 |
71119780 |
X |
+ |
28162770 |
MV411 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.4286728379965763 |
[146] |
[45] |
-7 |
hSpCas9 |
negative selection |
11884262 |
71123631 |
71123654 |
X |
- |
28162770 |
MV411 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-2.0063190414630077 |
[61] |
[12] |
-8 |
hSpCas9 |
negative selection |
11884263 |
71124305 |
71124328 |
X |
- |
28162770 |
MV411 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
1.0990121282124439 |
[178] |
[322] |
8 |
hSpCas9 |
negative selection |
11884264 |
71125083 |
71125106 |
X |
- |
28162770 |
MV411 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-1.5516497552912283 |
[173] |
[49] |
-7 |
hSpCas9 |
negative selection |
11884265 |
71125377 |
71125400 |
X |
- |
28162770 |
MV411 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-1.2761244052742375 |
[22] |
[7] |
-7 |
hSpCas9 |
negative selection |
11884266 |
71120160 |
71120183 |
X |
- |
28162770 |
MONOMAC1 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-0.19703684705955354 |
[133] |
[133] |
-2 |
hSpCas9 |
negative selection |
12053623 |
71126379 |
71126402 |
X |
- |
28162770 |
MONOMAC1 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-3.013729633696494 |
[154] |
[21] |
-9 |
hSpCas9 |
negative selection |
12053624 |
71125361 |
71125384 |
X |
+ |
28162770 |
MONOMAC1 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-2.9470585940512066 |
[147] |
[21] |
-9 |
hSpCas9 |
negative selection |
12053625 |
71132900 |
71132923 |
X |
+ |
28162770 |
MONOMAC1 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-2.3345403708094885 |
[109] |
[24] |
-9 |
hSpCas9 |
negative selection |
12053626 |
71134388 |
71134411 |
X |
+ |
28162770 |
MONOMAC1 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-2.090121643143042 |
[51] |
[13] |
-9 |
hSpCas9 |
negative selection |
12053627 |
71119757 |
71119780 |
X |
+ |
28162770 |
MONOMAC1 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.6888899433892286 |
[89] |
[31] |
-8 |
hSpCas9 |
negative selection |
12053628 |
71123631 |
71123654 |
X |
- |
28162770 |
MONOMAC1 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-2.31251406447949 |
[25] |
[5] |
-9 |
hSpCas9 |
negative selection |
12053629 |
71124305 |
71124328 |
X |
- |
28162770 |
MONOMAC1 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.5738291537249433 |
[142] |
[243] |
5 |
hSpCas9 |
negative selection |
12053630 |
71125083 |
71125106 |
X |
- |
28162770 |
MONOMAC1 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-2.373359619700017 |
[112] |
[24] |
-9 |
hSpCas9 |
negative selection |
12053631 |
71125377 |
71125400 |
X |
- |
28162770 |
MONOMAC1 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-2.93400244122576 |
[19] |
[2] |
-9 |
hSpCas9 |
negative selection |
12053632 |
71120160 |
71120183 |
X |
- |
28162770 |
OCIAML2 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-2.733664231075955 |
[35] |
[29] |
-9 |
hSpCas9 |
negative selection |
12222989 |
71126379 |
71126402 |
X |
- |
28162770 |
OCIAML2 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-2.829083796154637 |
[49] |
[38] |
-9 |
hSpCas9 |
negative selection |
12222990 |
71125361 |
71125384 |
X |
+ |
28162770 |
OCIAML2 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-3.29005757960034 |
[59] |
[33] |
-9 |
hSpCas9 |
negative selection |
12222991 |
71132900 |
71132923 |
X |
+ |
28162770 |
OCIAML2 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-3.7145554081282506 |
[44] |
[18] |
-9 |
hSpCas9 |
negative selection |
12222992 |
71134388 |
71134411 |
X |
+ |
28162770 |
OCIAML2 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-3.824266779856862 |
[22] |
[8] |
-9 |
hSpCas9 |
negative selection |
12222993 |
71119757 |
71119780 |
X |
+ |
28162770 |
OCIAML2 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-3.6632749031845573 |
[31] |
[13] |
-9 |
hSpCas9 |
negative selection |
12222994 |
71123631 |
71123654 |
X |
- |
28162770 |
OCIAML2 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-0.1201325781580278 |
[9] |
[50] |
-1 |
hSpCas9 |
negative selection |
12222995 |
71124305 |
71124328 |
X |
- |
28162770 |
OCIAML2 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.5443205162238104 |
[35] |
[290] |
5 |
hSpCas9 |
negative selection |
12222996 |
71125083 |
71125106 |
X |
- |
28162770 |
OCIAML2 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-1.148701730354799 |
[19] |
[49] |
-6 |
hSpCas9 |
negative selection |
12222997 |
71125377 |
71125400 |
X |
- |
28162770 |
OCIAML2 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-4.171069543383254 |
[12] |
[3] |
-9 |
hSpCas9 |
negative selection |
12222998 |
71120160 |
71120183 |
X |
- |
28162770 |
OCIAML3 |
viability |
GGAGTTACTCACCCATGAAAGGG |
MED12 |
ENSG00000184634 |
-1.4162205211088803 |
[60] |
[68] |
-7 |
hSpCas9 |
negative selection |
12392355 |
71126379 |
71126402 |
X |
- |
28162770 |
OCIAML3 |
viability |
GCAAGTGGTATGACATGCCAAGG |
MED12 |
ENSG00000184634 |
-1.8729835900269787 |
[90] |
[74] |
-8 |
hSpCas9 |
negative selection |
12392356 |
71125361 |
71125384 |
X |
+ |
28162770 |
OCIAML3 |
viability |
GCAGCCATGAGTGCAACCAGCGG |
MED12 |
ENSG00000184634 |
-5.5758602936139035 |
[78] |
[4] |
-9 |
hSpCas9 |
negative selection |
12392357 |
71132900 |
71132923 |
X |
+ |
28162770 |
OCIAML3 |
viability |
GGGCAGGATGAACAACGCGAGGG |
MED12 |
ENSG00000184634 |
-4.266432982295659 |
[50] |
[7] |
-9 |
hSpCas9 |
negative selection |
12392358 |
71134388 |
71134411 |
X |
+ |
28162770 |
OCIAML3 |
viability |
GCACCCAGCAGACCACGGAGTGG |
MED12 |
ENSG00000184634 |
-2.841935153767749 |
[18] |
[7] |
-9 |
hSpCas9 |
negative selection |
12392359 |
71119757 |
71119780 |
X |
+ |
28162770 |
OCIAML3 |
viability |
GAAGCCCCAAGTGAACCAGAAGG |
MED12 |
ENSG00000184634 |
-1.689164873364503 |
[46] |
[43] |
-8 |
hSpCas9 |
negative selection |
12392360 |
71123631 |
71123654 |
X |
- |
28162770 |
OCIAML3 |
viability |
AGAAAGGGAGCCAGAGGCGATGG |
MED12 |
ENSG00000184634 |
-0.44200454687911295 |
[8] |
[19] |
-3 |
hSpCas9 |
negative selection |
12392361 |
71124305 |
71124328 |
X |
- |
28162770 |
OCIAML3 |
viability |
TCAAAGGGAGAGGGAGGCCGGGG |
MED12 |
ENSG00000184634 |
0.2670159465270264 |
[48] |
[177] |
2 |
hSpCas9 |
negative selection |
12392362 |
71125083 |
71125106 |
X |
- |
28162770 |
OCIAML3 |
viability |
GCTGGTCGTAAAGAACCCCAAGG |
MED12 |
ENSG00000184634 |
-1.5550135087082995 |
[72] |
[74] |
-8 |
hSpCas9 |
negative selection |
12392363 |
71125377 |
71125400 |
X |
- |
28162770 |
OCIAML3 |
viability |
CAAACAGTACGACCAACCGCTGG |
MED12 |
ENSG00000184634 |
-3.33097323449037 |
[9] |
[2] |
-9 |
hSpCas9 |
negative selection |
12392364 |