Tag | Content |
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EnhancerAtlas ID | HS051-13657 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr19:10512790-10514050 | 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 | CCACTGCACT CCAGCCTGGG CGACAAGAAG GAAACTTCGT CTCAAAAAAA AAAAAAAAAA 60 AAAAAAAAGG AATACAACAG ACACTGGTAT GTAATGCAGG CACACTCATT TGGGGTAGCA 120 GGAGGTTAAA CCTTTAAGTC TTAGTCATCC CATTGGCTCG TGAGCACTGA GAGGGTGGTG 180 GGACATGGAT CACCCAGGCT TGGGATTCTG GGGTCTGGAT TCGGGACCTC TGTTGTGGTC 240 AGATAGAAGA AGGGGTGGTG AATTTAGAAT CAGACCAGGA GAGTCCCTGG ATAAGAGCAG 300 GGACAATTTG GGTCACAGAG TAGCTAACAG GCTGGGGACA AAAGGTGGGG TGGGTTTGGG 360 GTTCTGGGCT TGAGTTAGGG GAGAGTTTCC AATGCTGGCT GAGGCTCATA CAGGAAGCCA 420 GTCTGGGAAG TGGGTGGTGA CAGGGTCTGC AATACCAAGT AGGAGCAGGG GCTCTGGCTA 480 GGCCGGAAGC CACGTGGGCA GGATTTCCTG GTATAATGGG AAATGGGTCT ACCGGAGGCC 540 AAAGGAGAGG CTGGAATGTG AGGCTCTATC GGGTTGGAGC TGGTAGTTAG ATCCAGAGGG 600 GAACCAGATT CCAAAACCCA AGTACTCGGT GAGACTAAGG ATCCTGAAGG GGGACGGTTC 660 TACACTCTAG GAAGGGGGTC CTGGGTGTGG GCAGGGACAG GAATATCAGA GTAGCACAGA 720 GTTCCTTGTT CCGTTTAGAA AAGGAGTGGC GACTCCGGAT CTGAATGGGA ACCCCGGATC 780 AAGATCCCGG AAAGTAGATC CCGGGACAGA CCAAAGTATT GGGGGTCCAG ACTACGGAGG 840 TGGGGGGGCG ATGGGAGATC CCAGATAGGA AGTGAATACC CGAATAGGAT GAGGGATCAT 900 CTAGAAGAAT TTGGGGTCCA AACTTTGAGG CAGAGTTCTG GGTATAAATG TTAACTGCCG 960 AACAGAATTA GGGAGAACCC CCAAGACTCG TCTAGGGGAC TCCAGACTAT GAAGAAGTTC 1020 TAGGGGGTGA ATAGGGAATC CCACGCAAAA ATCGGAGCAG GGAGTGGGGG AGCGGAGATC 1080 CAGGGCAGGG ACTCAGGGTC CCAATGGTAC TGGGGTCCCG GAGTTGAATC GAAGCTCCTG 1140 AAAATCCAGA CTGGGGGGGT GAGAATCCTA GGTGTGAACA GCGGGGTCCC TGGGCAGTAT 1200 CGGGGATCAC AACTCCGAAG CGGGGTCCGG GAGTGGGGAA AGGGATGGGC GCGCGCGCCT 1260
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