Tag | Content |
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EnhancerAtlas ID | HS108-40465 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr9:19216280-19217470 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr9:19216290-19216300 | ACCACTTGAA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGACAGGAGA ACCACTTGAA CCTGGGAGAC AGAGGTTGCA GCGAGCTGAG ATCACGCCAT 60 TGCACTCCAG TCAGGGCAAC AAGAGTAAAA CTCCATCTCA AAAAAAAAAA AAAAAAAAGC 120 CTTACAATAA CAGTAAAATA CATCAGTTAC TATTAGTACT ATTATTATTT GCATTTCACA 180 GATGCAAAGA CCAAAGCTTA GAGAGATTAC ACAGCAAATG GTGGAGCTGG GATTTAAATA 240 CAGGCAGTTT TACTCCTAAT TCATTACACA GAGTGTTACA AGTTGCTATC TTATTCTTGC 300 TGATGTCACC CTGTTGTTCT CCAAGGTTAG TACTGTCTAA TGAAGCTTGG ACTAAAAATG 360 GTTTGTTCCA CTTATCTTGT ATTCATTACT GTCAGTTGAA AGACGCCACT TATCAGTGTC 420 CTTTTTGATT CTGCTTTGAG GGCAGTGGTG GAGACAGCTG ATATGCATTC TGTACCTTTC 480 TATATGTCAA CCATATTCTA GCCCTTAATC CCAAGATCTC AATTGGAGAG GAGTCTTTCG 540 AGAAGGAGGA ATGGTCAGGT TGTTGGAGGA AGTTTGAACT GTGAAGTAGA ATATCTAATT 600 GAGATAGCAG CAATGCTGGC AGGAAGAGAT GGAAGCCAGT GTTAGGATGG AGAGAAATGG 660 CAGTGAGGTG ATAATGAAAA TGCCTAATGA ATTTTGTTTG GTTTTCATTT AATCTTTCAA 720 CAATACCACA AGCTAAGTAC TTAACCTGAG AGGTTAGACA AACTTGCCCA AGTCCAAGCT 780 GGTAAATTGC AGAGCCAGAA TATGAACTCA CATCTGTTAG TCCATATTGT CTGAAGTGTC 840 TGTCACAAGG TTAAACCATT ATAACTGCCA TTATTTGGAA AAATAAAGAT ATTTATGAAT 900 AATGTATATT GCCAGTTCTG CTAAACGCCA CCTTGCCAGG CAGGAAAATT AATCTCACAG 960 AAAGCAAGGT GGCTGAATTT TAGCACATAG TCTAAAACTT GGCACTTTCA TATAAAGGAG 1020 AAAGTGACAA ACTTTAATAA GGCACTTGGT AGGGAAAATT TTTATCTTAA GTCCAAATTT 1080 ATCTCCATTA CAGTTAGTAT ATGTGCTGCC AAAGCGAGCA CATCTCCATT ACAGTTGAAA 1140 CCATGTTAGT GAGAAATGTG TTTGAAGAGG GCTGCTGCGC GCAGGACAAA 1190
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