Tag | Content |
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EnhancerAtlas ID | HS147-41652 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr9:2389770-2390730 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr9:2389818-2389828 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr9:2389818-2389828 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr9:2389818-2389828 | ATTTTCCATT | + | 6.02 | POU2F2 | MA0507.1 | chr9:2389809-2389822 | TTAATTTGCATTT | + | 6.25 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGACTATTT GAAAGTGTGG CAGTATAATT TTATGATTAT TAATTTGCAT TTTCCATTTA 60 TACCTATCCA ATCCACTGCA GTTTCCTTTC AAGAAGACAG CCTGAGCTTT TCTCTTCCCT 120 TGCCCTGGAG CTTTGGCAGG GCCAAAGGAG AAGTTGTTGG AAGAACAACG TTCTTTGTGC 180 ATGTGTTCAA AGACTCTGTC TTTGGGGGAG ATTGTGCTCA CTATCCTGGC TGGGGAGAAG 240 AGAGAGAAGA ATGCCTGGGA GCAAGACAAA GACTCTGTCT TTGGGTGAGA TTGTGCTCAG 300 TATCCTGGCT GGGGAGAGAA GAGAGAAGAA TGCCTGGGAG CGAGAGACAG GAGAGAGAGA 360 CGTTTCTTCA GGTAGAGAAG GGACTAAGGT TGGCAGTTCA CCAAGGAGTC AGGGATGCGA 420 ACCTGGTGAC CTAGATAGTG AGAACTCAGA GAGGTGATTC AGAGAAGCCT GCCCCAGGCA 480 CTGCTGCTTC TTGCTAGGCA AATGCCTCAG TTGGCACAGT AGCTATAGAG ATGTCAACAC 540 GTCAGATGCC ATGTAGGTTT GGAAAGTGAG GCTATCAGTG GCATCTATGA CAGCACATTA 600 GAAGCTATGT TCATTTTTTA TGGGCATCAT GTAAGGTTTC TGGACTACTC TAGGCAGAGG 660 GAAGAACTCC CATTAAGTAC TGATGGAATT TTCTGCCAGC TATAAAAATT GGGTCTTAGA 720 GTTAGATTTA ATTTGATTTT TAAAAATGTG ATATCTTTAA AATCTGTAGG ATAAAATGTA 780 TGTATTCACC ACAAAGTCTT TTATAAAGGA AAATAACATG AATGGGCTTG AGTTGTGACA 840 GGATAATGTT CGAGAAAATT CACCTGGCAT CCATGAACTT TATTGCAATT TGGGAATCAG 900 ATTTTTCCAG AAACTGAAAA AGGTGGATGA GGGACCAAAG GTAAAACCCA CAAAAGAAAC 960
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