Tag | Content |
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EnhancerAtlas ID | HS050-69397 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr9:96463730-96464900 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZBTB18 | MA0698.1 | chr9:96464426-96464439 | CAACATCTGGACT | - | 6.07 | ZNF263 | MA0528.1 | chr9:96464396-96464417 | GGGGGAGGGAGCTGAGGAGAG | + | 6.35 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGGGGGTGT GAGTGGAGAG GTCACCTGGA GCCATCCTTA GGGCCTTGCA GGTAGAGGGG 60 AGGAAACGGG AGGGATGAGT AAAGGAAGGA CTCACCAAGG CCACCCCAAA CCCTGTTCTA 120 TCCCTCCCTC TCCATTCCCA GGCCACGTGC TTGGATCTAT AAGGAGGACC TGGCCCCTCC 180 ATGAAGACCT GGATGTCACT GCCAAGGCCA ACCCTCTGAC CCCCCACCCC CATCCTCTCC 240 TTGGTCTCAG TCAACAGGCG GCAGATCAAA CGGCCCCCCA GGGCCTGGCC TTGCCCATCA 300 GGGAAACATC ACACTGCTCT GGAATGAGGT GATTTCAAGC AGCCGATGCA AGGAAATGGG 360 TATTTATGTA ACGGTGGGCA TGGTTTTTAT TTTCCCTAAT TTTCAGATTA CTTTCGATTA 420 GGCCTCTTTG GAGTAGAAAA GGCTTGAAGT GAAATCGATC CTGCCTAAAT CATTATGGCC 480 CGCCCAGCCC CAGGCCGCCT CTGCAGACAA TTACCCCAGA CCCCAGGGTT AGGGGGCAAA 540 CTCCAGGCGG GGGGATACTT CCTCAGAGCT CACCCAGCCC GGAGTGGCCA GGGCCCCGCT 600 GGATGGGGCC TTTTGTGCTC ATGTGGCACA CAGCGGTCAT TGATTCGGTC CCTCTGGCCA 660 GGGGGCGGGG GAGGGAGCTG AGGAGAGCAG TTCCCACAAC ATCTGGACTC TATCTCTTCT 720 TCCCACCCCC AGTCAGGACT GGGAGGGGGT GGGGAGAAGG AAAAGAGAAA ATGCCCAGGC 780 CAAATTCAAA TGCTTTCATA AATTTTGCAC TAGAAATGTT TTGACATGAA TATTTTTGTC 840 AGTCTCCAGC GTCTGCCCAA AGAAACTCAA CTCCACACAA CAGCTCGAAT ATATTTTCTG 900 GTTGACTCTG GAGCCACTTG CTGCAAGGCA GGCAAGCTGG GCCCAGGCAC CTGTGAGGAA 960 TGCCTGGGGC AGGCAGGGGC ACTGGAGACC CCAGTGACAT CTGGGGAAGG CCCAGGTGTG 1020 GCACCCCGCA GCCAGGGGGC GTCCTTCCAA GGTCCACCCA GGCGGGTACT GCCTGGGCTC 1080 CAGCCAAGCG GTGGGTGGCT GGAAGCCAGA CCCAGAGAGA TGCAGGGAAG GAGTGGATAC 1140 CTCGGGAGGA AACTCCACAC ATGTTAATAG 1170
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