Tag | Content |
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EnhancerAtlas ID | HS176-19143 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr19:45187710-45189030 |
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 | AGGGCACAGA GGTCCTCGCT GAGAAGGTGA CAAATGAGCA AAGACTTGTA GGAGGGGAAG 60 AAAGGAGCCA TGTGGGGCTC TGGAGGAAGA GCATTCCAGA CAGAGGGAAT AGCCAGTGCA 120 AAGGCCCTGG GGCAGAAGCA TGCCTGGCAT ATTCAAGGAG CAGCAAGGGG GCTGGGCATG 180 GTGGCTCACA CCTATAATCC CAGCACTTTG GGAAGCCAAG GCAAGCAGAT CATTTGAGGT 240 CAGGGGTTCA AGACCAGCCT GGCCAACATG GTGAAACCCC TTCTCTATTA AAAATACAAA 300 AATTAGCCGG GCATGGTGGT GGGCACCTGT AATCCCAGCA ACTGGGGAGG CTGAGGCAGG 360 AAAATCACTT GAACCCGGGA GGCGGAGTTT GCAGTGGGCC AAGATCGTGC CCCTGCACTC 420 CAGCCTGGGT GACAGAGCAA GACTCCACCT CAAAAAAAAA AAAAAAAAAG GAGCAGCAAG 480 GAGGCCAGTG TGGTGGAGAG GGTGGGGAAG GAGGAAAAGG TGGGTGGAAG TTGACGTCAG 540 GAGATGGACG GAGGGGCACA TGGCGCAGGG CCAGGTAAGG CACTGCCGAG ACTGTGGCTT 600 TGAGGGGCAG GGTGCTGTGA AAGGCGAATA ACGGCCCCCC AGTGACGTCT ACATCCTAAT 660 CCCCTGTGAA TGTTACGTTA TATGACAAAA GAATGCAGCC ATGATTAAGT TCAGGATCGT 720 GCTTTGGGGA GATTATCCTG GATTGCCCTG GCAGGCTCTT TATGTAATCA CACAGATCCT 780 TATAATCGAG AAGGACACAG GAAGCGTGAG TCAGAGGGGC TGTGACAACA AAGGAAGCAA 840 AGCCCTTTGA AGACGGGAGA AGGAGCTGAA AGTCAAGCAG CACTTCAGAG TCAGAATGAT 900 TGAGTGTGAG AGAGTCCATG GGCCATCGTG AGTGTTGAAG ACGGAAGGGG GCCTTGAGCT 960 AAGGAATGCA AGAAACTTCT AGAAGCTGGA GGAGGGCCAA GCTCAGTGGC TCACGCCTGC 1020 AGTCCCAGCA CTTTGGGAGG CCAAGGTGGG AGGATCGCTT GAGGCCAGGA GTTGGAGACC 1080 AGCCTGGGCA ACATAGCAAG ACCCCGTCTC TACAAAAAAA AAAAAAAAAA AAAACAGAAC 1140 CGAGGGTGGT GGCTCATGCC TGGAATCCCA GCACTTTGGG AGGCCGAGAC AGGGGGATCA 1200 CCTGAGGTCA GGAGTTCAAG AATCAGCCTG GCCAAGATGG GGAAACCCCG TCTCTACCAA 1260 ACATAGAAAA ATTAGCCAGG CGTGGTGGCG GGTGCCTGTA ATGCCAGCTA CTGGAGAGGC 1320
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