Tag | Content |
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EnhancerAtlas ID | HS024-04356 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr13:111997960-111999130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:111998578-111998596 | GTAGGGAATGAAGGAAGG | + | 6.73 | EWSR1-FLI1 | MA0149.1 | chr13:111998582-111998600 | GGAATGAAGGAAGGGAAG | + | 7.01 | MYC | MA0147.3 | chr13:111998702-111998714 | GGGCACGTGGCC | - | 7.22 |
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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 | TCAGTCACCT GGGATCTGAG CACTCCTTAG ACTGTCTTCA AATAAAGCCT TGGCCAATGA 60 CTGGGAATGG GTTTTGGCAA GAACCTAGAG CTGTGCAGAT GGGGCTCAGC GGCCCTAACT 120 GGCAGAGTCT CTTTGCACGA TGTTTCCAGC GTGGCCCGGA CCATCCCTTG CAGAGGTGAG 180 GCAGAATGGA TGACCCCACA AAATAACACT AAAAGCCAGG TTTGGCCGGA GGCACGCCTA 240 CTTCTTAGCT TTCATCCTCA GGAGGAAGCG GCACACAGAG CGGCCTCCCG GCAGCCACGC 300 TTTCTGGGCA GCTGGGTCTT TGCTGCCTGT GGCTCCTTTG GTGACTCCTC AGTCACTAGA 360 GAGCAAGTTA CTGGTGGAAC ACGTCCACCT TTGTGGGCCC CTTTGCTGAA GCCCTCAACC 420 CTGCCCCCTT CCCTGAAAAC AATCAAGATC CAGCCTGAAA AAAGTGCCAG GTTATTGGTG 480 GACTGGATGC TCGTCAGAGA CGTTAGGGGT CACCTGGGGC CTCCGGTTTG GGAAGCCCCT 540 GTGACTCACT AGGGTGTGGG TCGGGGGAAG GGCTTCCCCA TGTGTGGTTT GGGGACTGGC 600 CTTGCTAAGG GCAGTGGGGT AGGGAATGAA GGAAGGGAAG CAGTTCAGTG TGTAGCTGGG 660 AAGAGGACCG GGCCCTGGGG ACTGCTCCGG CCAGGGCCCC CCAGGAGAAG GGCCAGAACT 720 CCTAAGTACA AGTGAGGCCG GTGGGCACGT GGCCCCATCA GGGACAGCCA GCCATGGCCC 780 GGATGTGTGA CAACCCTGCA CAGGCCGGGG CCTCTGCCCT CGCGCAGTTG GTGCCCTGCT 840 GAGCGAGGCG AAGGCCAGAC AGAGCTGCCA AGGAAGCGCT TCCCAGGCAG TGGCTTCTCA 900 CAGAACCCCT GGCCGGCAGC CACGGGCACA GCTAGTCGTG GCCAAGCTCA GAGTCAGTTT 960 GGGAGAGGAC AACCCAAAGA CACAAACAAG CAGGCATGGT TTGTTGCGGT CACCAGATAG 1020 GCTGCCATAG CCATAAAATG TGTCTCTTGG TTAGAGGTGA CTTCGCTGGT GTCAGCAGAA 1080 GTACTGTGAG CAGGGAAGGC AAATACACAC CTGGGATATT GTCTATGGCT GCGAAGATTC 1140 AGTGTTGTTC CTTTCATGAT GGAAGGGCCC 1170
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