Tag | Content |
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EnhancerAtlas ID | HS133-14422 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr18:78003630-78005150 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr18:78004978-78004989 | GGGCGGGAAGG | + | 6.62 | RREB1 | MA0073.1 | chr18:78004508-78004528 | CCCGTGGGGGTGGGGTGGGG | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CCTCCCGCCC ATGCTTGTGG GCTCTTCCCC TCACCTAACC CACAGCTGGC ACACTTGATT 60 TGGGGGAGCT GGGGGCACTT CTGTGCTCCA GAGAAGATGG GTGTGGGGCC GAGGTCATGG 120 GGCAAGGGTA AGGACAGGAT CTTATGATAA ATGAGGGATT CATTAAAAGA CCGTGTACCC 180 CTAAGCAGAG AAGGATCCTG CAACTCACTG TAGCAGGCTG GAGAGGCGGC CATGCTGTTG 240 CTGGGACACC TCCCCGCCTC AATCCTCTGC AGACACCCTG GAAATCCTAC TCCAAAGGTC 300 AGAGCAGCAC AGCGAGAGGG GGCTGTTGGA CTTGCCTCCC CAGAGACAGG GGAGGGAACA 360 CCCGCCCTGC GCCCAAGATA GGCACACAGT TAGGGGTGCG GGCTCCCACT CCGCCGTTAG 420 GAGCCTTTCC CACAACTCTG AGAACCGGGG TGCGAAGAAA GAAAGGGCGA AAGGGCCGCT 480 CAACTCCCAG AGAGTAGCCA GCGAAAGACT CGAGGGGCCC CCTCCCGCAG GACCCCGAAC 540 AACTGCAGCA CCTCCTCAGC CCGCGGGGTC CACCAAGGAG ACCCTCACAA ACAATAGCAT 600 CTGCGGCGAA GGAACCACCC CCGCAAAGGG CAGAAGCGCC AGATCCTACC AGCCAATTAC 660 CCAGACGCGC ATCGCGACCC GCAAGTTCGG GCACGCTCCG CCCGGGCGCA GGCAGCGGGA 720 GGGGCCGGGC ACGCCCGTGG GGGTGGTCTG GGTACGGGTC TGATCCGGGG GCGCGCTCGG 780 GAGGGGTCTG GGTCTGAGCC GGGGGCGCGC CCGGGGGAGT GGGCTGGGTC TGGGGCGGGG 840 GCGCGTCCGG AGGTGGGGGA GTCTGGGGTG GGGGCGCGCC CGTGGGGGTG GGGTGGGGTG 900 TCTGGCCCGG GGACGCGCCC GGGGAGGCGT GGTCTGGGTC TGGGCCGGGG GAGAGCCGGG 960 TGCGTGCTCT GGGTCTGCGC GGGGGAGCGC GCCTGGTGCC TAGATGTTTG GTACCGAGCG 1020 GGTGGGGGAC GCCGGGCTCG GAGCCGGCGG CAAGTCTCCT CCTGGCAGGT AACAAGCCTC 1080 CTTTGCAGCC TTGAAGGCGC CTTGGCCAGG GCCATCCCAC GGCCCGGGCC CCCAGAGCCC 1140 CCCCACGGCC CCGAATCCGA GCAGCCCCTG GCCCTCAACT CGCCCCGGAA AGGCCGCCCT 1200 CCCCTCCAAT GTGTGGCGCG CCCCGATCGC CTCTCACTCG TGGAACAAAA GAGCAGCTCC 1260 CGCGGAGCGG GTCCAGAGTC TGCCCGGACT GTCCGATGGC CCTCGGCCCT CTGAGCGCCG 1320 CGGCTGCCGG GCTTTGTGTC CGCGCGGGGG GCGGGAAGGA CGGCCGGGGT CCCCAGTGCG 1380 CGTCCCGCGG AGCGGCGCGC GGCGCCCGAA CTGGAAAGTT GTCGCCGGCG CCTGTCGCCT 1440 CCACGCCGCC CCAGTCCCCC TCCGCGGGGC GCCCCATTCA TTAGCCAGGA GACTGGGCGC 1500 AGGGCCGCCG GGGCGGGCGG 1520
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