Tag | Content |
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EnhancerAtlas ID | HS184-08553 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:115100210-115101480 |
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) |
CTCF | MA0139.1 | chr12:115100576-115100595 | GCACCAGCAGATGGCGGCA | + | 6.4 | IRF1 | MA0050.2 | chr12:115101362-115101383 | GAAGAAAAAGTGAAAGAGACA | - | 7.2 | STAT1 | MA0137.3 | chr12:115100411-115100422 | TTTCCAGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr12:115100411-115100425 | TTTCCAGGAAATGG | + | 8.42 | ZNF263 | MA0528.1 | chr12:115100690-115100711 | TTTCCCCCATCCTCCACCTTC | - | 6.08 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I114662 | chr12 | 115099697 | 115101283 |
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Enhancer Sequence | TGCTCTTTAC AGCACATCTG CCTGTAAGGA TGTGGGTATC ATTATTCCAC TTTTATTTTA 60 TGAGGAATTA AGACCCAGAA AAGTTAAGCC ACCTGGCCAA AGGACACTCA AAAAGTAGGT 120 GGCAAAGCCA GGACTCCAGT CCCATTTTTC TGCCTCCAAA TTCTAGTTAT TTGCCTTGCC 180 ACCATTCTCT CTATCTCTTA GTTTCCAGGA AATGGCCATG GGGTTTGCTT CACTGGAATG 240 CAATTCCATG AGAACAGAGA CCATGTCCCA GTGATGATTA ATTGCTGAAT AAATGAATGA 300 TAACGTAAAT GAGTATGTGA CTCAGCCTTC CAGAAGTATT GGAAAAGCCC CATGCACTTT 360 CCTATGGCAC CAGCAGATGG CGGCAAAAGA GCAGCTTAGC AAAGGCAGAG GCAAACACTT 420 GGCGTTTCTT TCATTTATGT ATCCTCTCTT CCTTGATCTT TGCAAAACAG GTAGCTTGCA 480 TTTCCCCCAT CCTCCACCTT CACTACTCCC CTCCCCCCAT TCTGGGAGGA ACCAAGAGGT 540 AGTGCTCACA GACTGCAGTC CCCTCTTTCT GTTTTGACCT CTTTGCCCCA CCTCAGAGAC 600 AAGGTTATTT CAAGAAATGG AAGAAGAAAT AACACCAGAA GAACTTTAAT GGCAATGAAA 660 ACCAGTGCAG AAATGACCTT TTTATTGACA AATAGAGAAA AGGTATCATG TCCCCAGCTG 720 CTGATGAGGC AGACACAGAC TGTCCCCCAA CATTGGCCTC ATCATCCATA CTTTTGTGAT 780 TTGCCTTGAA GGGAAGTATG GGGTAGAATA GAGGTGGGCA GGGGGAATTT CTTGTTGCGA 840 GGAACTGAAA CGGAAGTGTT GGGGATGGGA TGGTGGCAGT GGAGAGGAGA GGGTAGCCTT 900 GGTTTACATC ATTTTGTTTG AAATCAGTCT TGATTTCCTT GACGCCAGGA GGAAATCCAT 960 CCCTAAGTGG CCAAGCACCA CCCAGAGGCA TTTATTTAGT CAGGGCCTAA GAGTGACAAG 1020 GGACTTCCCT GTGATCCTAT TTTAACAGAG GGGAGGAAAG AGGAATAACT ATCTTTTCCC 1080 TTGAACATTC TGCAGTGTCT AGACTATTCC TTTATGTCTG TGAATTTTCA TGTGTGGTTG 1140 GTATGTTTAC CTGAAGAAAA AGTGAAAGAG ACACAAGAAG GGCACAATGA TAGAGAGAAA 1200 ATACATCCAC TGCAACCACT ACAACCTCTG CCTTCCAAAT TAGTGGGATC CCTGGGCACA 1260 TTTAAACTTG 1270
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