Tag | Content |
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EnhancerAtlas ID | HS139-07516 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr10:98977600-98978650 |
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) |
EWSR1-FLI1 | MA0149.1 | chr10:98977927-98977945 | GGAGGGAAGGAAGGAAAT | + | 7.59 | EWSR1-FLI1 | MA0149.1 | chr10:98977923-98977941 | GAAAGGAGGGAAGGAAGG | + | 8.69 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH10I097217 | chr10 | 98977528 | 98978804 |
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Enhancer Sequence | GTTGGATATA TCTTCCAAAG AATGCCACTT TCTAAAAAGG ATAGTGTTTC CACTGCAACA 60 GTTTCAGTTC CCTGGATAGA ATCTTCTGCT CATGTAAGGA TCTCCCTTAA CACAGCTATA 120 AAAATAAACA GAATATTGCT GGGCATGGTG GTGTGTGCCT GTAGTCCCAG CTACTCAGGG 180 GACTAAGGGA GGATCACTTG AGCCCAGAAG TGGCTATTCA CGGGTGTGAT CACAGAACCT 240 GAACTAGCCA CCGAATAACC ACTGAACTCC TGTCTCCAGC CTGGGTAACA TATTGAGATC 300 CCCATCTCTA AAAAAAAAAG AATGAAAGGA GGGAAGGAAG GAAATGAGTA ATATTTAACT 360 GCATCAGAGG AATAACCTCT GCTTCTCTCA TGCTTAGTAT GCTAACTTGC TTTTCTTGGT 420 TCTCAAATGA TGCAATCTGA CAGAGCTGCA GCTTCCTGGT TGAGGGTTAT TTTTTCATGC 480 CTATATTTAA GATGCTTAAT TTTGTGATTC ATTCTTTATA ATTAGATATA ATGTTTAGAA 540 TATATCCATG TATATCATAT TCACATTTTT CCTTTGAGGG CTTTAATTTT CCCCTCTGAG 600 CTGATCTCAA CTGCAACCTT TTTTTTTTTT TTTTTTTTTA AGACAAGGTC TCACTCTGTC 660 AGCCAGGCTG GAGTGCAGTG GCATGATCTT GGCTCACTGC AGCCTCCACC TGCTGGGCCC 720 AAGTGACCCT TCCACCTCAG CCTCCTGGGT AGCTAGCACC ACAGGCACAC ACCACCACGC 780 CCAGCTATTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TATTTTTAGT AGAGACAGGG 840 CTTCACCTTG TTGCCCAGGT TGGTCTCGAA CTCCTGAGCT CAAGTGATCT GCCTGCCTCA 900 GCCTCCCAAA GTGCTGGGTT TACAGGTGTG AGCCATGGTG CCTAGCCTCA ACTGCAACCT 960 TAAATTTGCA ATTGCCATGA GTCAAGAGAG CCCCAGCTGT GTCCATGTGG AAAACTGACA 1020 TTTCCCCCAA GGTCGGTGTG TGTGTGTATA 1050
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