Tag | Content |
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EnhancerAtlas ID | HS184-04628 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:103989360-103989940 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:103989685-103989704 | AGACCACGAGGTGGCGCCG | + | 6.44 | SNAI2 | MA0745.2 | chr10:103989573-103989583 | AACAGGTGCA | + | 6.02 | ZNF263 | MA0528.1 | chr10:103989894-103989915 | GGAGGATGAAGGGAAGAGGAC | + | 6.17 | ZNF263 | MA0528.1 | chr10:103989891-103989912 | GGGGGAGGATGAAGGGAAGAG | + | 6.74 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH10I102229 | chr10 | 103989392 | 103992010 |
|
Enhancer Sequence | GGATTTGGGG GGAAAGAGGG CTGCTGTGAT GGCAGGAGGC TGCTACCAAG GGGATGATCT 60 GCAGGTGGGA CGCCTGAGGG TGTGTGGAAG GGTGAGAGGC ACACACACAG ACACTGAAAG 120 AATCCTAGGC CTGGTAGGCA CTTAACAAAT GTCTGTTACA GACCAGAATT TTATTGCTGT 180 TAGAGACCCA AGCCCCTCAT AGGAACAGTG AGAAACAGGT GCAGAAAGGC GGAGTAACTT 240 TATCTAAAGT CATAGGCTCC CTGAATAGCA GAGCTGACAC CTACAAGGAA GCGTTGGAGA 300 CCAGATCTAC CAGCTAGCCT CCCTGAGACC ACGAGGTGGC GCCGCAGCAC CGGCTGTGGC 360 CGATGCCAGC CAGGTAGCCG GTTTCCCACG TCCCCCGCAC GCACGCACCT CTTTGCTGCA 420 GGAATCCCGG GCTGCCCCGA CCTGGAGTAG GGGGGGTGGT GAGTGGGACT GAGTCCCTAG 480 AAGCCTGGAC CCTCACTTCG TTCCTGTACA TCCAGCTCGC CTGTAGACAG TGGGGGAGGA 540 TGAAGGGAAG AGGACTCAAG CGCAACTTTG AATCATCACG 580
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