Tag | Content |
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EnhancerAtlas ID | HS175-13413 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr19:45187910-45189020 |
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) |
HSF1 | MA0486.2 | chr19:45188681-45188694 | GAAACTTCTAGAA | - | 6.25 | Nr2f6(var.2) | MA0728.1 | chr19:45188913-45188928 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr19:45188201-45188222 | GGTGGAGAGGGTGGGGAAGGA | + | 6.04 | ZNF263 | MA0528.1 | chr19:45188213-45188234 | GGGGAAGGAGGAAAAGGTGGG | + | 6.16 | ZNF263 | MA0528.1 | chr19:45188216-45188237 | GAAGGAGGAAAAGGTGGGTGG | + | 6.62 |
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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 |
GH19I044683 | chr19 | 45186982 | 45190472 |
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Enhancer Sequence | CAGCACTTTG GGAAGCCAAG GCAAGCAGAT CATTTGAGGT CAGGGGTTCA AGACCAGCCT 60 GGCCAACATG GTGAAACCCC TTCTCTATTA AAAATACAAA AATTAGCCGG GCATGGTGGT 120 GGGCACCTGT AATCCCAGCA ACTGGGGAGG CTGAGGCAGG AAAATCACTT GAACCCGGGA 180 GGCGGAGTTT GCAGTGGGCC AAGATCGTGC CCCTGCACTC CAGCCTGGGT GACAGAGCAA 240 GACTCCACCT CAAAAAAAAA AAAAAAAAAG GAGCAGCAAG GAGGCCAGTG TGGTGGAGAG 300 GGTGGGGAAG GAGGAAAAGG TGGGTGGAAG TTGACGTCAG GAGATGGACG GAGGGGCACA 360 TGGCGCAGGG CCAGGTAAGG CACTGCCGAG ACTGTGGCTT TGAGGGGCAG GGTGCTGTGA 420 AAGGCGAATA ACGGCCCCCC AGTGACGTCT ACATCCTAAT CCCCTGTGAA TGTTACGTTA 480 TATGACAAAA GAATGCAGCC ATGATTAAGT TCAGGATCGT GCTTTGGGGA GATTATCCTG 540 GATTGCCCTG GCAGGCTCTT TATGTAATCA CACAGATCCT TATAATCGAG AAGGACACAG 600 GAAGCGTGAG TCAGAGGGGC TGTGACAACA AAGGAAGCAA AGCCCTTTGA AGACGGGAGA 660 AGGAGCTGAA AGTCAAGCAG CACTTCAGAG TCAGAATGAT TGAGTGTGAG AGAGTCCATG 720 GGCCATCGTG AGTGTTGAAG ACGGAAGGGG GCCTTGAGCT AAGGAATGCA AGAAACTTCT 780 AGAAGCTGGA GGAGGGCCAA GCTCAGTGGC TCACGCCTGC AGTCCCAGCA CTTTGGGAGG 840 CCAAGGTGGG AGGATCGCTT GAGGCCAGGA GTTGGAGACC AGCCTGGGCA ACATAGCAAG 900 ACCCCGTCTC TACAAAAAAA AAAAAAAAAA AAAACAGAAC CGAGGGTGGT GGCTCATGCC 960 TGGAATCCCA GCACTTTGGG AGGCCGAGAC AGGGGGATCA CCTGAGGTCA GGAGTTCAAG 1020 AATCAGCCTG GCCAAGATGG GGAAACCCCG TCTCTACCAA ACATAGAAAA ATTAGCCAGG 1080 CGTGGTGGCG GGTGCCTGTA ATGCCAGCTA 1110
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