Tag | Content |
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EnhancerAtlas ID | HS050-45841 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr3:9189140-9190040 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr3:9189855-9189876 | GGAGGAGGAGGATAAAGGGAT | + | 6.61 | ZNF263 | MA0528.1 | chr3:9189837-9189858 | GGAGAAGGAGGAGCAGGAGGA | + | 8.09 | ZNF263 | MA0528.1 | chr3:9189852-9189873 | GGAGGAGGAGGAGGATAAAGG | + | 8.44 | ZNF263 | MA0528.1 | chr3:9189840-9189861 | GAAGGAGGAGCAGGAGGAGGA | + | 8.94 | ZNF263 | MA0528.1 | chr3:9189843-9189864 | GGAGGAGCAGGAGGAGGAGGA | + | 9.73 | ZNF263 | MA0528.1 | chr3:9189846-9189867 | GGAGCAGGAGGAGGAGGAGGA | + | 9.83 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATGAACTCG GCTGTCAGGT GCTGTAGCCA CAACCTGAGC CCCGGACTAG GTGAGCCCAG 60 ACTGAAGGCT CCCTGCCCCT AAATCTCAGC CACCTCAGCT TGTCACTCAT CAGTGCATCA 120 AAATCCCTGA TTCTGGGCAC AGAATCATTA GCCAGATGAG CCCTTCCAGG GAAGATTCCA 180 GGCAGAATGA TTCATGAGAG AGGAAAGAAA AATAACAATG TGCTCGCAGC AAGAAGCATC 240 CAAGCGCTTC CTTTTGCTCT GCGGGAATTG GATGCATTCT GGCCCAGGTG TTTCCACACA 300 GCCGTCCAGA GTGGTGGCCT CTGGAGAGAG GTGAAGCCTC CAGGAGAAAG GAATGCAGCC 360 TGTGCCAGAG CCACTAAAGC AGATGACATG GGCAGGCCAG GGTCCACCAG GGCTGTGATG 420 GGGCCCAGAC CCTCAGATGG TGTCACCACA CTCTGGCCTC TCCCTCCCAT CTTTCAGAAG 480 CCCCTCTGCA AAGTTTGGGA ATAAAAGGCA TTAAGCCTCA CCTCCCACGC CTGAGATTGT 540 CTCCAGAGCC AGGGAGGGGC TGTTTTGTTG GTTTTCTTCC TCCAAAGCCA GTGAGAGAAA 600 TACCCACGGA TCCAGTTTAG CTTAAGTGTC CAAGAGAACC TCCATTAGCA TCTCAGGGAG 660 GACAACGCTA ATCACCAAGG GCATCAACTT CAGGGAGGGA GAAGGAGGAG CAGGAGGAGG 720 AGGAGGATAA AGGGATGAGG GCGGAGATGC CTGCCTCTCC TCCAGAAACG CCGGCTTTTA 780 TTTCAGGGAC TGGAAGAAGA AAACGCCCTA GAAAAACCAT CAACCCCAGC ATTTCTCTGT 840 GCTAGGCAGA AAACAAGCAG AGGAATGTGT GCTACAAGCA CCAGCAATTT TGGGGGCAGT 900
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