Tag | Content |
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EnhancerAtlas ID | HS052-18718 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:19151200-19152040 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr19:19151552-19151562 | CTCAAGTGGT | - | 6.02 |
| | 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 |
GH19I019039 | chr19 | 19149929 | 19152036 |
| Enhancer Sequence | CTCATTTGTA CAAGGGAGGC AGGTTAAGTG CTAGGTTTTT TTTAAAAAAA TTGTTACTAA 60 TTATTGTAGA GACAGTGTCT CGCTACGTTG GCCAGGCTGG TCTTGAACTC CTGGATTCAA 120 GTGATCCTCC CATCTCAGCC TCCTGAGTAG TAGCTGGGAG TACAAGAGCA TGCCACCACT 180 CCCTGCCAAG AGCTGGATTC TTGGCCAGTT TTCAGAAGCC TGAGCTGTAT TTGTTTTAGT 240 ATTATGAAAG CACAGAGTTT GACTTTTTTT TTTTTTTGCA ACATCGTCTG ACTGTCAGCC 300 AGGCTGGAGT GCAATGGCAT GATCTCGGCT CACTGCAACC TCCGCCTCTG TGCTCAAGTG 360 GTTCTCCTAC CTCGGTCTCC CTGATTGCTG GGATTACAGA CGTGAGCCAC CACACCTGGC 420 CCAGATTTTG ATTTTGATAT GTACTGGATT TTTTTTTAAT GCTCACTTGT CTCATCTGTA 480 GCTACCAGGC ATCCCTTAGG GTTTGGAAGC TTCCTTGCTT CCTGGTCTCA CAAGACCCCA 540 GCGTTACCTG CCCCATGACC TGCTGGGACT TGGAATCAGC CATTCCTCCA GAAGCCCTGG 600 CTCCTTGTTT TTAAAGATTT TATGTAGAGA CAGGGCCTCC CCATGTTGTC CAGGCTAGTG 660 TTGAACTCCT GGCCTCAAGC CATCTTCCTG CCTCAGCCTC CCAAAGTGCT GGGATTACAG 720 GAGTGAGCCA CCTAGCCCTG GCCCCAGCTC CTTTTCGTGG GAAATGGTAG AAACCATACA 780 TGGTGTTAGA GGTATTCAGT GCTCCTGTGC TGTCATTTCT CCTAGGCATT TTTAGTTGCT 840
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