Tag | Content |
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EnhancerAtlas ID | HS133-22775 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:115231220-115232570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr3:115232088-115232109 | GGAGGAGTAGGAGGAGGTTGG | + | 6.39 | ZNF263 | MA0528.1 | chr3:115232085-115232106 | GGGGGAGGAGTAGGAGGAGGT | + | 7.48 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH03I115512 | chr3 | 115230961 | 115232710 |
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Enhancer Sequence | AGATCTGTTG AGTACATGAA AAATTGAGAG GAGGAAGACC CTGACCCTGG GGTGTCTTGG 60 ACTACTTCTC CTCTGAATGT TCCTAGGCTA AAACCAAACA TTTTTAATAG ATAATCTGTT 120 CCCTTAGCCC CTTCTGTTTC TACCTCGTCG CGTGCCCTCT CTGCCTAAAC GCTCTCTCCT 180 CCTCCCCAGG TTCATATTAA TAAGGAGAAG GTCTCCCCGC AGCTCCTCTG GACCGAGCCA 240 CACCTCTGCC TGGGAATCCT GGGCTGGGGC TGCAGAAGCC CGCTGCGCGC CTCCTGGTTT 300 CTATGGAGAC CCTGCTTGAT GTCAATGGCG GCTCCGGAGC GCAGGGAAAC CTAAGCGTTT 360 GTATTTAAAT GAGGGAAAGT GGGGGAAGGG GAAGTAAAAG AGGAAGGGAA CAGAAGAGAG 420 GATGGTAGAG GTGAGCGGGC GGGTGTTGAA CTCTGGGGAC TAGAAAAATC CAGCTGCGTT 480 ACTCAGTCAT CTCATGCTCG CGGAGAAATC AGAGGAAGCA GCAGCGGGCA GAGGGGTGTT 540 TATTTCTTGC GTGAGAAATA TCCGACTTCT TTCTGACATC CGGGAGTAAG GGACAGGCAA 600 CTAGGAATCC CTTTTCATGT GGCTGGCCCC TGGCTGATAG TGCTGCTCGA TTTCATTTCC 660 AAGAAGAAAG GGAGAGTTCT CTCTTTGCCC AGAGACTCAA GTCTTAAAGA TTCATTGCTG 720 CTATGGGAGG GGCCACGCCT CTATCTTTCA CTCTCGACCC TTTCCCCTGC AGCATAACTA 780 AATAGAAGCT CTGGAAAGAC GGATTCGAAA AGTTCTGGGG TCTGGATTAA CTGCTGTTTA 840 TTGGCTGACA CCCTAGCAAG AGGCTGGGGG AGGAGTAGGA GGAGGTTGGG CAGAATGTAT 900 GCTATGATTG AATTGCACGA GGGTTCAGAT GACGTCAGCT TGAATAAAGG TCTGACCTAG 960 TGAATGTTAA ATGTGGCTGA GTGACTGAAT CCTTGGAAGG GATCGATGGC AGAAACCTCC 1020 ATGAAAGGAC CATGCCACTT CTTTAAAATA TTAAGCATGT GATTCTGCTG ATCTCCCCTG 1080 CAACTCCCAG AGCGCTGGTG GAATCTTAGC TTTCTGCTAT AATCACTTGA ACATTACTTA 1140 CTGCCCTAGA TAACTGCGGG TCACGTGGAG TTTGCACCAA AAAAGGAAGT CTTTGAAAAA 1200 AAGAAAAAGC CATTAATCAA AGTGCCTGCT AATCTTACAA AGTGAAAGCA ATTCAATTTA 1260 ATAAACACTT TCAGAGGACT ACTTCGAGCC AAGTGTATGC AAAATGAGTG AGATGTTCTT 1320 TGCCTTCAAG GTGCATACAT TCTGGCTGGG 1350
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