Tag | Content |
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EnhancerAtlas ID | HS146-07720 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr19:45188090-45188780 |
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 | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I044683 | chr19 | 45186982 | 45190472 |
|
Enhancer Sequence | GGCGGAGTTT GCAGTGGGCC AAGATCGTGC CCCTGCACTC CAGCCTGGGT GACAGAGCAA 60 GACTCCACCT CAAAAAAAAA AAAAAAAAAG GAGCAGCAAG GAGGCCAGTG TGGTGGAGAG 120 GGTGGGGAAG GAGGAAAAGG TGGGTGGAAG TTGACGTCAG GAGATGGACG GAGGGGCACA 180 TGGCGCAGGG CCAGGTAAGG CACTGCCGAG ACTGTGGCTT TGAGGGGCAG GGTGCTGTGA 240 AAGGCGAATA ACGGCCCCCC AGTGACGTCT ACATCCTAAT CCCCTGTGAA TGTTACGTTA 300 TATGACAAAA GAATGCAGCC ATGATTAAGT TCAGGATCGT GCTTTGGGGA GATTATCCTG 360 GATTGCCCTG GCAGGCTCTT TATGTAATCA CACAGATCCT TATAATCGAG AAGGACACAG 420 GAAGCGTGAG TCAGAGGGGC TGTGACAACA AAGGAAGCAA AGCCCTTTGA AGACGGGAGA 480 AGGAGCTGAA AGTCAAGCAG CACTTCAGAG TCAGAATGAT TGAGTGTGAG AGAGTCCATG 540 GGCCATCGTG AGTGTTGAAG ACGGAAGGGG GCCTTGAGCT AAGGAATGCA AGAAACTTCT 600 AGAAGCTGGA GGAGGGCCAA GCTCAGTGGC TCACGCCTGC AGTCCCAGCA CTTTGGGAGG 660 CCAAGGTGGG AGGATCGCTT GAGGCCAGGA 690
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