Tag | Content |
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EnhancerAtlas ID | HS095-15332 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:45187630-45189100 |
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 | GCGTTGTCTG TCAGATGGGG ATAAGTGTAT TGGGGAAATG GAGGGGGGTC GAGAGTATTG 60 GGGGACTGAG ATTTTTAATT AGGGCACAGA GGTCCTCGCT GAGAAGGTGA CAAATGAGCA 120 AAGACTTGTA GGAGGGGAAG AAAGGAGCCA TGTGGGGCTC TGGAGGAAGA GCATTCCAGA 180 CAGAGGGAAT AGCCAGTGCA AAGGCCCTGG GGCAGAAGCA TGCCTGGCAT ATTCAAGGAG 240 CAGCAAGGGG GCTGGGCATG GTGGCTCACA CCTATAATCC CAGCACTTTG GGAAGCCAAG 300 GCAAGCAGAT CATTTGAGGT CAGGGGTTCA AGACCAGCCT GGCCAACATG GTGAAACCCC 360 TTCTCTATTA AAAATACAAA AATTAGCCGG GCATGGTGGT GGGCACCTGT AATCCCAGCA 420 ACTGGGGAGG CTGAGGCAGG AAAATCACTT GAACCCGGGA GGCGGAGTTT GCAGTGGGCC 480 AAGATCGTGC CCCTGCACTC CAGCCTGGGT GACAGAGCAA GACTCCACCT CAAAAAAAAA 540 AAAAAAAAAG GAGCAGCAAG GAGGCCAGTG TGGTGGAGAG GGTGGGGAAG GAGGAAAAGG 600 TGGGTGGAAG TTGACGTCAG GAGATGGACG GAGGGGCACA TGGCGCAGGG CCAGGTAAGG 660 CACTGCCGAG ACTGTGGCTT TGAGGGGCAG GGTGCTGTGA AAGGCGAATA ACGGCCCCCC 720 AGTGACGTCT ACATCCTAAT CCCCTGTGAA TGTTACGTTA TATGACAAAA GAATGCAGCC 780 ATGATTAAGT TCAGGATCGT GCTTTGGGGA GATTATCCTG GATTGCCCTG GCAGGCTCTT 840 TATGTAATCA CACAGATCCT TATAATCGAG AAGGACACAG GAAGCGTGAG TCAGAGGGGC 900 TGTGACAACA AAGGAAGCAA AGCCCTTTGA AGACGGGAGA AGGAGCTGAA AGTCAAGCAG 960 CACTTCAGAG TCAGAATGAT TGAGTGTGAG AGAGTCCATG GGCCATCGTG AGTGTTGAAG 1020 ACGGAAGGGG GCCTTGAGCT AAGGAATGCA AGAAACTTCT AGAAGCTGGA GGAGGGCCAA 1080 GCTCAGTGGC TCACGCCTGC AGTCCCAGCA CTTTGGGAGG CCAAGGTGGG AGGATCGCTT 1140 GAGGCCAGGA GTTGGAGACC AGCCTGGGCA ACATAGCAAG ACCCCGTCTC TACAAAAAAA 1200 AAAAAAAAAA AAAACAGAAC CGAGGGTGGT GGCTCATGCC TGGAATCCCA GCACTTTGGG 1260 AGGCCGAGAC AGGGGGATCA CCTGAGGTCA GGAGTTCAAG AATCAGCCTG GCCAAGATGG 1320 GGAAACCCCG TCTCTACCAA ACATAGAAAA ATTAGCCAGG CGTGGTGGCG GGTGCCTGTA 1380 ATGCCAGCTA CTGGAGAGGC AGAGGCAGGA GAATCGCTTG AACCCAGGAG GCGGAGGTTG 1440 CAGTGAGCCA AGGTTGCACC ATTGCACTCC 1470
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