Tag | Content |
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EnhancerAtlas ID | HS187-11334 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr18:20629430-20630310 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr18:20629658-20629679 | GGAGGAGGAGGAGGAGGAAAG | + | 10.19 | ZNF263 | MA0528.1 | chr18:20629655-20629676 | GAAGGAGGAGGAGGAGGAGGA | + | 11.01 | ZNF263 | MA0528.1 | chr18:20629667-20629688 | GGAGGAGGAAAGGAGAAGAAA | + | 6.63 | ZNF263 | MA0528.1 | chr18:20629664-20629685 | GGAGGAGGAGGAAAGGAGAAG | + | 7.42 | ZNF263 | MA0528.1 | chr18:20629652-20629673 | AAAGAAGGAGGAGGAGGAGGA | + | 7.66 | ZNF263 | MA0528.1 | chr18:20629661-20629682 | GGAGGAGGAGGAGGAAAGGAG | + | 8.5 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGCACTGCA ATCTAGATGA CAGAATGAGA CCCCGTCTTT AAAAAAAAAA AAAAAAATTA 60 ACCAGGTGTG ATGGCTCACA TCTGTAGTCC CAGCTACTCA GCTACTCGGG AGGCTGAGGC 120 AGGAGGATCA CTTGAGCCCT GGAGTTCAAG GCTGCAGTGC ACTATGACTG CACTACTGCA 180 CTCTAGCCTG GGTGACAAAG TGAGATCCTG TCTCAAAAGA AAAAAGAAGG AGGAGGAGGA 240 GGAGGAAAGG AGAAGAAACC AAAGAAAGCA TATTCATCAT ATAGTTCATA AATGTATTTG 300 GTATTTAATT CTACAGTCTT AAAAGTTGCC CGGGGGAAAA AAATTTAGCT TTCCTTTCCT 360 TTCACTGATT TTATCTCATG AGCCACCATT TCTGCCCAGC AACAGGAAAT GACATCTTAC 420 CAATTAAAGG TAACCCAATG TCTCCTGCAG TAAACAGTCA ACTAGTGACT CTCTCTCTCC 480 CTCACTATTC TGGAAAATGC CTGAGCTGCA GGGACCTGTG TCTCGCAAGA GGGGGATCTT 540 AATCCACACT CACTGGTTTT CTCCCTATTG ACTTTTTCTG CTATGGGCTG GCCCCAGGGG 600 TCTTGACAGC CCAGCCTCCC AGATGTGAGG TCAGCAATCC CACTGGCCTG TGCACTCCAT 660 GTCTCTGCCC ATCTGGCCAA TCCTGGAGGC AGACAGGAAG GCTCCCTGTG TTCCCAGGCT 720 TCACACAAGT AGAGGGAGGC ATGGCGGGTG GAGTGGGAGA GAGACAGAGT CTCTCGGCCT 780 CTCTATGCTT CCACCTGCCC TGCTGTCATT TCTGCCCATT TGACCACACC CCACTCTAGG 840 CAGCCGCCAT CCTCTCACAG AGTTGCAGGT GGGAAGTGGG 880
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