Tag | Content |
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EnhancerAtlas ID | HS184-11465 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr15:71363210-71364460 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr15:71363622-71363634 | TGCCCTAAGGCA | - | 6.04 | TFAP2C | MA0524.2 | chr15:71363622-71363634 | TGCCCTAAGGCA | + | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_43479 | chr15:71362741-71364009 | MCF-7 | SE_45794 | chr15:71361796-71364290 | Osteoblasts | SE_64706 | chr15:71362726-71363628 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I071070 | chr15 | 71362962 | 71364348 |
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Enhancer Sequence | AACTGAAAGT GGGAAAGAAG CCATGGTCTG AGGAATTAAC ATAAAAACTC TGAGAAGGCC 60 AGAGGAGACC AAAGACAGTT GTGAGCTGGT TTAGAAGCTC ATAGCAGTCT GGGATTGGGA 120 CACAGTGGGG CAGTAGGTGC AACGTGGTGG GTAAATTTTG CTTTTAACTG TCCCCTACAT 180 TGCTTTGGCA GGATCACTTT TCTGGCCTCA TCACTTCTGC AGAACAGAAA TTAGCAAGAG 240 CAGCCCAGAT GCCAGGGGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 300 TGTGTGTTGG AAGGTGGGAC AGAAAGGTTG GGGAGGTGGG GAGAATATCA TTGCAACCTC 360 AAGATCCTGC CAGGTTGAGA ATCTGGTGAG AATACATGTT ATGATGACTA GTTGCCCTAA 420 GGCATTTATT TCTTCATTCC CTTTCTCTCC AGGCCCTCAA CAAATTGGAT TGCAACCTAA 480 TATTTAAGGA AGAGTCCCTG AAGGAGGAGA CGCCTGGTGC AGACACTGGG AATGAAGTTG 540 GTCTGCAGGT TCTGTGGTGT GTGGTGCTTG AACTCGTGGA GACTTTCCCC ACCTTTCTGC 600 ATAAATAGTT CTAAAGATCT ACATTGTACA GACTATGTTC TCTTACCACA GTGCAATTTT 660 GTTAGAAATA AATTACAAAA GAATAATTGC TGGGAGAGAA TGCTGCATGG ATTTCTCATG 720 TTTCTGTATG TCTTTTGAGC AGAGGCATTG TTAGCTTTTG TTCTGGCCTG TATTTTCAAG 780 GATGTTTATA TAGCAAACAG CCTTGGAAAA TAAAAATAGT ATCTCCCTTC ATGGCAGAGG 840 GCAGGTTTAT TTGCTGTCCA GTAAAATGAA GATAATATCT CCCACTGGGG CAGAAGTTGG 900 GTGGGTTGGC TCACAGCCTC CTTATTGGAG TTTCCTAAAC TCAGGGTTCC TCAGCTGTGA 960 CTTAACCCCA CCTCCAGCAT CCTCCTGGAC CCAGGTATGT ATCACTCTTG TGGGGCTTGT 1020 GAAGCAAGGG GAACTAATGA GAAATGAAGT AATTAAGTTC TTTGTCTCTG ATCCAGGAGT 1080 CTCATGTCTT CTGCCAGCAT TTTTGAAACT GTGACTGGCT GGTTTGTTAA CTTGCAAGTA 1140 AGATCAAATT TAATACTCTT CACAGTTCTT CGTAATAGGT TTTTAAAAAT TCCATAAATC 1200 TGGATATTAA ATAGCATAAA ACTAAATAAT CATTAGATTA AAAAGAAACT 1250
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