Tag | Content |
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EnhancerAtlas ID | HS092-13481 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:115775330-115777790 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MITF | MA0620.2 | chr12:115776175-115776193 | CAAGGTCACATGACCCAC | + | 6.42 | MITF | MA0620.2 | chr12:115776175-115776193 | CAAGGTCACATGACCCAC | - | 6.42 | RORA | MA0071.1 | chr12:115776173-115776183 | ATCAAGGTCA | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I115337 | chr12 | 115774870 | 115777260 |
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Enhancer Sequence | AAAAAAAAAA AAGAAGAAGA ATAATCTGCT ATTTAAAATT AGAGCCCAAG AATTAATTGG 60 CAAAAAAAAA AAAGAAGAAG AAGAAGAAGA AAAAAGAAGA AGAATCTGCT CTTTAAAATT 120 AGAGCCCAAG AATTGGCAAA AAAAAAAAAA AAAAAAAAAG AAGAATCTGT TATTTAAAAG 180 AGCATTCCCG GGTGGCCCTG ATGATGGAGA ACTGGGGTGA GCATGCTTAC AAAAAACACT 240 AAGCGTTTGC TTAGATGAAT CATGCACTGA AAAGCAATGA AAGACGTCAT GGGAAAGGCT 300 GGCAGGAAAC TCATGAGTAG GGAGGAGCCA AGTCATGTCC CTGGCAGGAC AGTCCTTCAG 360 CCACTTTAGG GTGTCCCTGG AAGGGACAGT GACTAGATAG GCATGGTGGA GTGTTGAGAA 420 CAACAGATCT CATTGGGAAA GCGTCTACTA TGTGCCAGGT GGTTCCCTTG GGTTAACTCA 480 ATTCTTTCAA CAACTCTTAC ATCTGTCCCC TCCCCATCAG AATGCAGCAG GGAGGAGCAG 540 AGCTTGCCTA CCAATGGGCG GGATGCTGGT GTCAGGGTTT GTGTTCTTGC CACTTCTTCG 600 CAGAACCCGC ATGAAGATCC GGGAGTTTGG GGCATGGAAA AACTGGGACA CAGAGGGTGA 660 ACTGGGCTCA GAGTGGAGAA GGGACCCGTG GGTGTTCAAG GCCTCAAGAC CCAAATAGGT 720 CTGGAGGAAA AGAGCCTGGC TTTCCAGCCA GCTCTTGATC ATGTTGACTG GCTGATTTCT 780 CAAGAGTCCC AAGGGGAAGT TCTCAGATTT CCAATTCTAA GCAAGGGAAT AATGGTTCTT 840 AGTATCAAGG TCACATGACC CACTCTGCAG CGCACCTGTA TCGGGATCCA GAGCCCGGTG 900 CCTCAGTTCT TGCTGTGGTT TGGCAAAGAG ATTCCTGCTA CTTCAATTTT CACTGAATGG 960 CCACCCCTGA GCATGCAGAT GAGGCTTGAT AAATTATAGC TGAATTCCCC TGGTGCCCAA 1020 ATCTTTTTTT TCCTCATTTA CAGTACTTTA GCACTGACAG TAATAAAAGC AAAAATTGTC 1080 ACAGGTAGAC ACTTTCTCCA TTGAAAATGA TTTAATCTTC CCAGCATTCC TGTGGTAATC 1140 ATGTGAGAAT TAATGCATAT TTCACGGAAA TTTCACATCT ATCAAACGTT ATACCCATTT 1200 TAGAGATGTG GAAATCAAGG CTCAGGAAGA CTATATGATG TTTTTCCTCA AATTGTAAAG 1260 TTATAAGTAG AGGAGGCAGG ATGTTAATGA TACATTTAAC CACCGTGACA TGAGCCTTTT 1320 TAGTTTCAAA ACACTCACTC ATGTATGATT TCGTTTGCAC CTTACTTACA GCAACCTGTG 1380 GTTTGTTCAA TGGTAAAGTC CTGGTTCTCA AAAGTGATTT CCAGACCAGC AGCATCCACA 1440 GCGCTTGAAC TTGTTCAAAA TGCAAATTTA TCGGGCTCAC TGCTAGACCC AATGACTCAG 1500 AAATTTGCAG AAAGAGAGAT TCAGAAATCT GCATTTTAAC AAGCCCTCCA GGCTATTGTG 1560 ATACAAACTC ACAGTTGAGA ATGAGAGTGT AAGGAATTCT TTTTATAGAT GAGGGAACAA 1620 ACGGACAGAG AGGTCAAGCA GCCTGTCCAA GGTTGCAGAG GCAGTGGTTG CGGAGCTGGG 1680 CCTTAACCCC ATTGTTTATG GTTTCTAATG AGAGACACCT GGGAGAAGCA TTAAAATGCA 1740 GTTTCCCTTG TCCTCTCTAG ACCGACTGAC TCAAGATCTC CAGGGCTAGG GCCCCAACTT 1800 TGTCTTTCAG CAAACTTCCA GGTGAGTCTA GAGTTTTAGA ATTCTTCCAT AGTTCCTGTT 1860 GGACTATACT CGTGTAGTTA TTTTCTCTTC CCACTGTCCA GTTTCCTTCT TTTCTTTCTC 1920 CCACATCCCT TCATTTTTTC CCCTTCTCCT ATACTTTGGG CCTCTCTCCA AAACTAGCTA 1980 GTTGTTCATA ACTAGTTTGT TGCAGAGAAA CTAGAAGAAA CCCAGGGTAC CATGTCTTAT 2040 ACCTCTCCGT TTTTAAGCTG GTTAATAAAA AGTAATTAAA AGTCATCCAC AAATATGTTT 2100 GTTGTTAGAA TTTCAAACAG TGTAGAATTT TAGAGATTTT TAGAGAGTAA AAGCTGTTTT 2160 TCTTCTGATC CTTCCCAAAA CCAGGCCACC CCCAATTACT GTTAATAGTT TAGTGTGTAA 2220 CGTTCCAGAC ACCTACATTT TTTATTCGAA TAAATATATG CAGATACACA CTCAGAGGAT 2280 AATTCAAAAC AGAAATGGAA CTACACTATT CCTATTATAC TGTGACGTGG CTCACTTATA 2340 GATATTTTAT ACATTCCTTT GTGTGATTTT GTTTGTTTTT TATTTATTTA TCTTTTTTTA 2400 ATTTTACTTT AAGTTCTGGG ATACATGTGC AGAACATGCA AGTTTGTTAC ATAGGTATAC 2460
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