Tag | Content |
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EnhancerAtlas ID | HS139-09589 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:62248150-62249060 |
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) |
Nr5a2 | MA0505.1 | chr11:62248871-62248886 | CCTGGCCTTGGGCTT | - | 6.16 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I062479 | chr11 | 62246688 | 62249768 |
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Enhancer Sequence | AAAAGAAAAA AAAGAAAGGC CTGACTCTTT CTCAGTGGTC CTGGACTCTG AAACCCTGAC 60 CTCTGTCCCC AAACAGGGCC TTCCTTCCTG AGCTCTCTGC TATGCAAGGA ATTCTGCGTG 120 CAGTTAAAAA AAAAAAAAAA AAAAAAAAAC CTGGATTTGC TGCCTTCTGG TCTGACCAAG 180 TTGGAATGCG CAGCGTGAAG AAATGCTCGT TGCCTAGGCA GGAACAGCCA TCCACAGGAA 240 AACAGACCTC AGTAAATAAT GTCCTCGACC TTCCCCCAAA AGCCCAGAGG CTGCCTCCTG 300 TGAGTAACCG ATGAAACCCG AGGCGCTCCT GTAGCTCCTG GGCTGATCCC TCTCCAGGAG 360 ATGACTTGGA TGAGAAGGAA GGTGCTATGG GCTTCTCTTT TCTTTTTTTG GTTTTTTTTT 420 TTTTGGTTTT TTTTTTGTTT TTTTGAGACA GAGTTTCGCA CTTGTTGCCC AGACTGGAGT 480 GCAGTGGCGC AGTCACGGCT CACTGCAACC TCTGCCTCCC GAGTTCAAGC AGTTCTCCTG 540 TCTCAACCTC CCGAGTAGCT GGGATTACAG GTGCCCACCA CTGCACCCAG CTAATTTTTG 600 TATTTTTTAG TAGAGACAGA GTTTCACCAT TTTGGCCAGG CTGGTCCTGA ACTCCTGATC 660 TCAGGTAATC CACCCACCTC GGCCTCCCAG AGTGCTGGGA CTACAGGAGT GAGCCACTGT 720 ACCTGGCCTT GGGCTTCCCC TTTCTTCCAT TTCCCTTGCA CCATCTTTGT CTGGACCCTC 780 AGGGTCTCGT CCCTGCCTCC ACACCTCCCA CCCTCAAACC TACCATTGCT ACCCAAAAAC 840 CTCCCTAGAC CTCAGCTTCT AGCAAGTCAC CCTTCAATAC TCTTTATTTT TTATTTATTT 900 ATTTATTTAT 910
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