Tag | Content |
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EnhancerAtlas ID | HS101-21027 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:10512300-10514050 |
Target genes | Number: 16 | 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 | CTCCAGTGGC TTGCTTGGCA GGTACACTAC CCAGGAGACT CAGGATTTAA GGAATAGGTC 60 TGGAAGTGGG ACTGGGAGCT AGATGAAGAG ACTAATGCCG TATTCCAGAG TATTCTGGAA 120 GGATGGGAAA GGGACCTTCT AGTTGTTTCT GGATAAATGA TGGGGAATTG CCCTATGGGA 180 GGGTGGGGTA AGAGATCCTC ACTAGAAGGT TCTGAGAGGT ATATGCCCTT CGTTTAAGAG 240 CACAACATGG CTGGGTGCGG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCCGAGG 300 TGGGTGGATC AACTGAGGTC GGAAGTTCAA GACCAGCCTG ACCAACATGG AGAAACCCTG 360 TCTCTACCAA AAATACAAAA TTAGCCAGGC ATGGTGGTGC ATCATGCCTG TAATCCCAGC 420 TACTCAGGAG GCTGAGGCAG GAGAATCACT TGAACCCGGG AGGCAGAGGT TGCAGTGAGC 480 CAAGATTGTG CCACTGCACT CCAGCCTGGG CGACAAGAAG GAAACTTCGT CTCAAAAAAA 540 AAAAAAAAAA AAAAAAAAGG AATACAACAG ACACTGGTAT GTAATGCAGG CACACTCATT 600 TGGGGTAGCA GGAGGTTAAA CCTTTAAGTC TTAGTCATCC CATTGGCTCG TGAGCACTGA 660 GAGGGTGGTG GGACATGGAT CACCCAGGCT TGGGATTCTG GGGTCTGGAT TCGGGACCTC 720 TGTTGTGGTC AGATAGAAGA AGGGGTGGTG AATTTAGAAT CAGACCAGGA GAGTCCCTGG 780 ATAAGAGCAG GGACAATTTG GGTCACAGAG TAGCTAACAG GCTGGGGACA AAAGGTGGGG 840 TGGGTTTGGG GTTCTGGGCT TGAGTTAGGG GAGAGTTTCC AATGCTGGCT GAGGCTCATA 900 CAGGAAGCCA GTCTGGGAAG TGGGTGGTGA CAGGGTCTGC AATACCAAGT AGGAGCAGGG 960 GCTCTGGCTA GGCCGGAAGC CACGTGGGCA GGATTTCCTG GTATAATGGG AAATGGGTCT 1020 ACCGGAGGCC AAAGGAGAGG CTGGAATGTG AGGCTCTATC GGGTTGGAGC TGGTAGTTAG 1080 ATCCAGAGGG GAACCAGATT CCAAAACCCA AGTACTCGGT GAGACTAAGG ATCCTGAAGG 1140 GGGACGGTTC TACACTCTAG GAAGGGGGTC CTGGGTGTGG GCAGGGACAG GAATATCAGA 1200 GTAGCACAGA GTTCCTTGTT CCGTTTAGAA AAGGAGTGGC GACTCCGGAT CTGAATGGGA 1260 ACCCCGGATC AAGATCCCGG AAAGTAGATC CCGGGACAGA CCAAAGTATT GGGGGTCCAG 1320 ACTACGGAGG TGGGGGGGCG ATGGGAGATC CCAGATAGGA AGTGAATACC CGAATAGGAT 1380 GAGGGATCAT CTAGAAGAAT TTGGGGTCCA AACTTTGAGG CAGAGTTCTG GGTATAAATG 1440 TTAACTGCCG AACAGAATTA GGGAGAACCC CCAAGACTCG TCTAGGGGAC TCCAGACTAT 1500 GAAGAAGTTC TAGGGGGTGA ATAGGGAATC CCACGCAAAA ATCGGAGCAG GGAGTGGGGG 1560 AGCGGAGATC CAGGGCAGGG ACTCAGGGTC CCAATGGTAC TGGGGTCCCG GAGTTGAATC 1620 GAAGCTCCTG AAAATCCAGA CTGGGGGGGT GAGAATCCTA GGTGTGAACA GCGGGGTCCC 1680 TGGGCAGTAT CGGGGATCAC AACTCCGAAG CGGGGTCCGG GAGTGGGGAA AGGGATGGGC 1740 GCGCGCGCCT 1750
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