Tag | Content |
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EnhancerAtlas ID | HS113-13017 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr15:81321570-81322420 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr15:81322142-81322157 | TTGCTGAGTCATCGT | - | 6.04 | MAFF | MA0495.3 | chr15:81322142-81322157 | TTGCTGAGTCATCGT | + | 6.16 | MAFK | MA0496.2 | chr15:81322140-81322159 | TTTTGCTGAGTCATCGTTG | + | 6.13 | NFE2L1 | MA0089.2 | chr15:81322141-81322156 | TTTGCTGAGTCATCG | - | 7.8 | Nfe2l2 | MA0150.2 | chr15:81322143-81322158 | TGCTGAGTCATCGTT | - | 7.51 | ZNF263 | MA0528.1 | chr15:81321708-81321729 | GAAGGAGGGAAAGGCTGGGAG | + | 6.06 |
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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 |
GH15I081029 | chr15 | 81321741 | 81322942 |
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Enhancer Sequence | TAGCCCCCAT ATTCTCATCT TCTAATTATC CCCAACAGGG GTGCTTCACT TAAATAAAAT 60 TTCCCCAGGT TTCTCAGGAA TAAAATCGGA ATGGCTAGAG TTTCTCACCA GGGAACCTCC 120 CCAATGAGGA TAAGGAGTGA AGGAGGGAAA GGCTGGGAGT AATTGGACAA GGAACATAGA 180 TTTTAGAAAA GGAGAGTCAG CAAGAAATAG GTGTCATGCT AGGGTCAGAG GATCTCAAAG 240 GGTCTATATT GCTTCAGGAC TGGGAGGGTC TGAAAAATGA AATTCCAGTC ATGTAATTGT 300 GACTCAGCCT GTGGAATGAA CTTTGTGTGC TCACTCATAC ACGTTCTTTT CCTTCCTGGT 360 ACTCACTTGC CTACCCCCTT GTAGTTAGGT GGGGCCATGT GATGAATTCT GGCTGGTGGT 420 TTGTGAGTGG AAGTAATGTG TATCACCCCT ATGCTGAAGC ATTTACCTGC TGGTATAAGA 480 CCCTTGAGCA CTCTCTTGCC CTGCTGCATT GATGAAGAAG GCCACCTGTT TCAGTGGTGC 540 AATATAGGAT GTTGAGCCTT TGTCAACCTG TTTTGCTGAG TCATCGTTGC TTTGTCAGCC 600 TATTTCGTGG GTCATCACTG GTTGAGTGAT CAAGACTTAA ACATTGTTTG TCATTGCTTT 660 AACTAGGAGC AGTGTTTGTT ATTGCAGCAA AAACTAGCTT ATCCTGACTA ATATATTGCA 720 CAGTGAGAGA GGGAAGGAGG AAGCATGGAG GGAATTAGTG AAGCTTCTTG GAAGCTCCTC 780 CAGGTACAGA CTTAGACCAT ATATAAAAGA TGGAGGAAGC AGGGCTGCCT CCAAACAGAG 840 CTCAGGAAGA 850
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