Tag | Content |
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EnhancerAtlas ID | HS105-38896 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr19:10512700-10514050 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:10513843-10513864 | GGAGCAGGGAGTGGGGGAGCG | + | 6.17 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCATGCCTG TAATCCCAGC TACTCAGGAG GCTGAGGCAG GAGAATCACT TGAACCCGGG 60 AGGCAGAGGT TGCAGTGAGC CAAGATTGTG CCACTGCACT CCAGCCTGGG CGACAAGAAG 120 GAAACTTCGT CTCAAAAAAA AAAAAAAAAA AAAAAAAAGG AATACAACAG ACACTGGTAT 180 GTAATGCAGG CACACTCATT TGGGGTAGCA GGAGGTTAAA CCTTTAAGTC TTAGTCATCC 240 CATTGGCTCG TGAGCACTGA GAGGGTGGTG GGACATGGAT CACCCAGGCT TGGGATTCTG 300 GGGTCTGGAT TCGGGACCTC TGTTGTGGTC AGATAGAAGA AGGGGTGGTG AATTTAGAAT 360 CAGACCAGGA GAGTCCCTGG ATAAGAGCAG GGACAATTTG GGTCACAGAG TAGCTAACAG 420 GCTGGGGACA AAAGGTGGGG TGGGTTTGGG GTTCTGGGCT TGAGTTAGGG GAGAGTTTCC 480 AATGCTGGCT GAGGCTCATA CAGGAAGCCA GTCTGGGAAG TGGGTGGTGA CAGGGTCTGC 540 AATACCAAGT AGGAGCAGGG GCTCTGGCTA GGCCGGAAGC CACGTGGGCA GGATTTCCTG 600 GTATAATGGG AAATGGGTCT ACCGGAGGCC AAAGGAGAGG CTGGAATGTG AGGCTCTATC 660 GGGTTGGAGC TGGTAGTTAG ATCCAGAGGG GAACCAGATT CCAAAACCCA AGTACTCGGT 720 GAGACTAAGG ATCCTGAAGG GGGACGGTTC TACACTCTAG GAAGGGGGTC CTGGGTGTGG 780 GCAGGGACAG GAATATCAGA GTAGCACAGA GTTCCTTGTT CCGTTTAGAA AAGGAGTGGC 840 GACTCCGGAT CTGAATGGGA ACCCCGGATC AAGATCCCGG AAAGTAGATC CCGGGACAGA 900 CCAAAGTATT GGGGGTCCAG ACTACGGAGG TGGGGGGGCG ATGGGAGATC CCAGATAGGA 960 AGTGAATACC CGAATAGGAT GAGGGATCAT CTAGAAGAAT TTGGGGTCCA AACTTTGAGG 1020 CAGAGTTCTG GGTATAAATG TTAACTGCCG AACAGAATTA GGGAGAACCC CCAAGACTCG 1080 TCTAGGGGAC TCCAGACTAT GAAGAAGTTC TAGGGGGTGA ATAGGGAATC CCACGCAAAA 1140 ATCGGAGCAG GGAGTGGGGG AGCGGAGATC CAGGGCAGGG ACTCAGGGTC CCAATGGTAC 1200 TGGGGTCCCG GAGTTGAATC GAAGCTCCTG AAAATCCAGA CTGGGGGGGT GAGAATCCTA 1260 GGTGTGAACA GCGGGGTCCC TGGGCAGTAT CGGGGATCAC AACTCCGAAG CGGGGTCCGG 1320 GAGTGGGGAA AGGGATGGGC GCGCGCGCCT 1350
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