Tag | Content |
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EnhancerAtlas ID | HS108-20986 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr19:50440690-50441740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr19:50441692-50441706 | GAGGCCGAGGCGGG | - | 6.01 |
| | 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 |
GH19I049937 | chr19 | 50440601 | 50442410 |
| Enhancer Sequence | GCAACCTCTG TCTCCCGAGT TCAAGCGATT CTCCGGCCTC AGCCTCCTGA GTAGCTGGGA 60 CCACAGGTGC ACACCACCAA GTCCAGATAA TTTTTGTATT TTTAGTAGAG ACGGGGTTTC 120 ACCATGTTGG CCAGGCTGGT CTCGACTCCT GACCTCACGT GATCCGCCCA CCTCAGCCTT 180 CCAAACTGCT GGGACTATAG GTGTGACCCA CCGCGCCGGG CGCGAAATGA TTTCTTACTG 240 TGAGTCATGG TCAGAAAAGT TTGAAAGCCA CTGGTAGGCT CCCCCCAGCT TGACATACTG 300 ATTTTCAGAC AATAGCCGGT TTGCAGACCC CACGCTTCCA AAACCAATCA TTTCTGGCCT 360 CTGGGCGGAG TTTGTCTTAG CAGGAGTCTG CCGCCAGGTG GCGCGCGTAC CCCGCCGGGA 420 GTGGGTTTTG CTCCATCCCA GACTCAGACC GTCCAAGCCG GTGATTTCCT TCTGGTCGGT 480 TTACGGGGAC TAGAAGCCCT GACTTCGAAT ACAGTTCACA AAGCAGACCC CTGCAGGGGG 540 TTTTAGGCGG CTAAGAAGGG AATTGGCTCT CCTAAGACTC TCTTTCTCCA GAGAGCTCAT 600 TAAATGCCTC CCGCGCCAGA AGGGGTCCCC GCCCCCGGAG CTCGCATCCC AGTGGGGAGG 660 ACACACACAA ACCCCATTCG CGATCCCGTC AGTGCAGGGA GGCTCCGGCC TGGGGCCGAA 720 GAGCCGAGTC TCTCTGGTGC CTGACAGCAC GGGATAGAGC CCCGCCCGGC CACCTGCTGG 780 CTGTGTGACC TTGGGAATAG TGCTTGGCCT CGCTGTGCCT TGGTTCCCTC CACTATAAAA 840 TGGCAGTGAT AACAGCAGCC ACTTCATAGG GTTCCGGGCA TTGCGTAAGT TAATACATGC 900 AAAGCGCTCA GAAGGGATGG TGCATGTTTG TCGAACCCGT TGTTAAAAAT TCCCATTTTA 960 GGCTGGGCGC AGTCACTCAC ACCTGTAATC CCAGCACTTC GGGAGGCCGA GGCGGGCGGA 1020 TCACCTAAGG TCAGGAGTTC GAGACCAGCC 1050
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