Tag | Content |
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EnhancerAtlas ID | HS053-00380 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:15294700-15295950 |
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) |
RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26798 | chr1:15294684-15296104 | Esophagus | SE_53292 | chr1:15293321-15296336 | Spleen |
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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 |
GH01I014967 | chr1 | 15294172 | 15298701 |
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Enhancer Sequence | ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC ATGCGCAGTT CACAAGAGGG 60 TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC AGACAGGAGG TGGAGCTCCG 120 GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT GAAACTTCGC TCGCTCGCCC 180 CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG GACCAGTACC AGTCCATGGC 240 CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT CACTTTGTTA CAACAAGAAT 300 GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG CCCTAAACAC TGCCCTCTCT 360 CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA AACGCCTGCA GGGCACAGCA 420 GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG CATGGAGCAG AAGAAAGGAT 480 CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG GGAGCCTTTT CCCTGCCACA 540 GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT ATTATTTAAT TTGCTCATTC 600 ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT GCCGATGCCT GTGGTTCAGA 660 GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA ACCTACGACA CACTCAGTGT 720 ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC CTGTAGATGA GAGTCTATCC 780 CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG TCCAGCGGGG 840 TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC CATGCCCTGG CTGCCTTTGC 900 AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT GTTGAATAGA 960 ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC TTTCTTAGAC ACACATCCTT 1020 GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG TTTCCTGTGT CCCTTCCCAC 1080 ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA CGTGTTCATC TTCTATGCAG 1140 TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA AATTCATACG CTTGAAGCTA 1200 CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC 1250
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