Tag | Content |
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EnhancerAtlas ID | HS133-09661 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:101083830-101085310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr14:101084364-101084375 | AAAACAAAGAC | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_25635 | chr14:101082708-101086535 | DND41 | SE_33398 | chr14:101082203-101087486 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I100616 | chr14 | 101083291 | 101085337 |
|
Enhancer Sequence | TCAGCTCAGA GCTCACCGGG TAGCTGCTTC CTGGTAGATC TGTGTTAGGG TGCCACCCTG 60 GAAAGTTGGA GTGAGGGAAA AGGGGAGTGG GGGAGGCTGT GCACAGGAGA GCGCAGGAGA 120 AGCACAGCCT TTGTTCTGTC TCCTGGGATG ACTTCAGAGG CTGCCTGAAA ATTCTTATGT 180 GGAGCATGTG TATGGGCGGT GGGAGGGAGA AGAAATGATC CCAAACTCTT GTCTCCTATT 240 GGTCAAAGCA ACTGGGGAGA TCCCTAACCT CTAGAGAAAC TGGAGTGACA GATGCTGGTT 300 CCCCTTGGTG TGCGTGGGAG GGAGGCAGCC TGGGTTAGAA GCTGCGTTTT GCGGGAGACC 360 TGGCAGGCTG GACTGGACAG GGCTTCCTGG GCAAGAACTC CTGGGGGCAC CCGGCTTCCT 420 TCCGGCTGTC GAACTTCCTA AATGAACATC CAACATATCC TTCTTATGAG GAAGAGAGAA 480 GCCTTAAGGA CTTTGGTCCC TGGGATGGGA CCAGAACCAG TAGAGTTTGA GCTAAAAACA 540 AAGACCGCCT TAAGGAGGGC CGGCTTTCAG AAAGCCTCGC TTGTTTGGGA ACCTTCCTAA 600 AATAACACTG TTCGAAAGCT AAGACAAGAG CTCAGTTGTG CAAACCATAG GGAGTTTTAA 660 TCTGTGTGCC TGCTTGCGCC TGCCAGCTCG GCACGTGCTC GGAATCGGAG GCCAGTCTCT 720 GGAGGGTTCT CTGCTGGAGT GGCTTGAATG AGGCCTTCAT GCAGAAGCAG ATCCCACCCT 780 CACTTCTCTG AAGGATGATA GCAGGCTCCA GGGCCCTGAG TGGGGCACTG ATCAAATGCG 840 TGGGTCCTTC TTAGGATCTT TTTAATGGGT TGCTCCTTTT TAAATGATGC TCAGTTCTCA 900 GTGGGCGTCT CTGCCCTTCT GAAAGACGAG GCTGCCTCCT GCCCACCCTC ATCGTAGGCA 960 GCCAGGGTCC TGGCACGGGG AGGGAGCTGC CACTGCCGAG GAGTGTCTCT TCCTGTGAGC 1020 AGCTGCGGCT GGCTGCCCAG AGCTTTCTGG GGAAGTAGGA TCAGAGCTGT GGCTCTGATG 1080 GGGTTTTCTC TGCCCTGGCG GGAGGGGTGA GAAAAATGAA GAAGTCAGGT CACTGCTACT 1140 CTTCCTGGGA GGAAGACTGG GGGAAACGTT ATAATGTTTT GGCTCAAATC CTCTTTGTGA 1200 GAAGGTTCTG TGAGTCCAGA AAGGATAGGG TCACCATCTG ACTTCTAAGG GTGATTGGAC 1260 TTTGGGTGCC AGTAGAGCCT CCCAAGATTC TGCTGCCAGG GGAGGGTGGT GGGGGTTGGT 1320 CACAGCAGGA GCTGACATTT TCTGTCAAAT GCTGCCTTGT TTGTCATTGC ACCCAGAAAA 1380 TTAATGGTGG TAGCAGGAGC AGTTTCTGCC AGCCAGGCTC GCTGCTAAGC ACACGAGCGC 1440 CTTTAAGCCT CACCGCAGCC CTTATCCTCA CTTCCAAATG 1480
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