Tag | Content |
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EnhancerAtlas ID | HS091-08005 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:66188830-66189590 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr11:66189299-66189320 | AGCTCTGTCCGCGGTTCTGAA | - | 7.73 | REST | MA0138.2 | chr11:66189337-66189358 | AGCTCTGTCCGCGGTTCTGAA | - | 7.73 | REST | MA0138.2 | chr11:66189178-66189199 | GCTACTGTCCGCGGTGCTGAA | - | 8.55 | REST | MA0138.2 | chr11:66189221-66189242 | GGCGCTGCCCATGGTGCTGAC | - | 9.35 | REST | MA0138.2 | chr11:66189261-66189282 | GGCTCTGTCCATGGTTCTGAA | - | 9.78 | SCRT1 | MA0743.1 | chr11:66189457-66189472 | GGTCAACAGGTGTTT | + | 6.1 |
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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 |
GH11I066421 | chr11 | 66188985 | 66189810 |
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Enhancer Sequence | CATGCTGGGG CTACCGCAGA TCCGAGCTGC CAGGCGCCGG AGACCCTGGA GCTGAGGGAA 60 CCCGCTGGGG CTGTCGCATG TCTAGGGCAG CGTGCTGGCG AGCTGGGGAG ATTCGGGACT 120 CGGGAGATTC GGGACTTTCT ACTTTTCCTC CTGAGCTCCC TCCAGACCTC ACCTTAGTTC 180 TGAATGAGAG TTAGAGAGCC TGGACGGTGT CCCTAACACC AGATTATGAG AGGATAAGAG 240 CCAGGACAGA GCGGCCTCGG TGCCCGCCAG TGCAGAAGCG CTCCGGGAGC CGGGGAGGGA 300 AGCCCGGGAA GTTGCAGGGA TGGAGCTGCC TGAGCCTAGG GGAACATAGC TACTGTCCGC 360 GGTGCTGAAA GGGATCTCCT GTCGCCTTCG GGGCGCTGCC CATGGTGCTG ACGGCTGCGC 420 CGGCCGTGTA TGGCTCTGTC CATGGTTCTG AACCCACAGT CGGCTTCGGA GCTCTGTCCG 480 CGGTTCTGAA ATTCAGAGCC GCTTTGGAGC TCTGTCCGCG GTTCTGAAAT TAAGAGCCGA 540 GAGGAGCCGA CCCCGCTTTA GAAGTCGAGG GCTTGTGGGC TATGGAGATA CAGCAACAGG 600 TTCCCTGGCC AAGAGCTGCG GGCAGCGGGT CAACAGGTGT TTGCAGAGGC AGGTCCATGA 660 GAAATTCCTC TGGATTCTCT GAAACTCAGA CCATGCCTTC CTCACTTCTT CTCTGCCTCC 720 CAGTCTTACT CCTGACGCAC TACGTCTTCT CGCCCTACAG 760
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