Tag | Content |
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EnhancerAtlas ID | HS073-07279 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:10512860-10514050 |
Target genes | Number: 15 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:10513843-10513864 | GGAGCAGGGAGTGGGGGAGCG | + | 6.17 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AATACAACAG ACACTGGTAT GTAATGCAGG CACACTCATT TGGGGTAGCA GGAGGTTAAA 60 CCTTTAAGTC TTAGTCATCC CATTGGCTCG TGAGCACTGA GAGGGTGGTG GGACATGGAT 120 CACCCAGGCT TGGGATTCTG GGGTCTGGAT TCGGGACCTC TGTTGTGGTC AGATAGAAGA 180 AGGGGTGGTG AATTTAGAAT CAGACCAGGA GAGTCCCTGG ATAAGAGCAG GGACAATTTG 240 GGTCACAGAG TAGCTAACAG GCTGGGGACA AAAGGTGGGG TGGGTTTGGG GTTCTGGGCT 300 TGAGTTAGGG GAGAGTTTCC AATGCTGGCT GAGGCTCATA CAGGAAGCCA GTCTGGGAAG 360 TGGGTGGTGA CAGGGTCTGC AATACCAAGT AGGAGCAGGG GCTCTGGCTA GGCCGGAAGC 420 CACGTGGGCA GGATTTCCTG GTATAATGGG AAATGGGTCT ACCGGAGGCC AAAGGAGAGG 480 CTGGAATGTG AGGCTCTATC GGGTTGGAGC TGGTAGTTAG ATCCAGAGGG GAACCAGATT 540 CCAAAACCCA AGTACTCGGT GAGACTAAGG ATCCTGAAGG GGGACGGTTC TACACTCTAG 600 GAAGGGGGTC CTGGGTGTGG GCAGGGACAG GAATATCAGA GTAGCACAGA GTTCCTTGTT 660 CCGTTTAGAA AAGGAGTGGC GACTCCGGAT CTGAATGGGA ACCCCGGATC AAGATCCCGG 720 AAAGTAGATC CCGGGACAGA CCAAAGTATT GGGGGTCCAG ACTACGGAGG TGGGGGGGCG 780 ATGGGAGATC CCAGATAGGA AGTGAATACC CGAATAGGAT GAGGGATCAT CTAGAAGAAT 840 TTGGGGTCCA AACTTTGAGG CAGAGTTCTG GGTATAAATG TTAACTGCCG AACAGAATTA 900 GGGAGAACCC CCAAGACTCG TCTAGGGGAC TCCAGACTAT GAAGAAGTTC TAGGGGGTGA 960 ATAGGGAATC CCACGCAAAA ATCGGAGCAG GGAGTGGGGG AGCGGAGATC CAGGGCAGGG 1020 ACTCAGGGTC CCAATGGTAC TGGGGTCCCG GAGTTGAATC GAAGCTCCTG AAAATCCAGA 1080 CTGGGGGGGT GAGAATCCTA GGTGTGAACA GCGGGGTCCC TGGGCAGTAT CGGGGATCAC 1140 AACTCCGAAG CGGGGTCCGG GAGTGGGGAA AGGGATGGGC GCGCGCGCCT 1190
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