Tag | Content |
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EnhancerAtlas ID | HS051-04848 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr11:66188960-66189440 |
Target genes | Number: 36 | 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 |
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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 |
GH11I066421 | chr11 | 66188985 | 66189810 |
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Enhancer Sequence | GGGACTTTCT ACTTTTCCTC CTGAGCTCCC TCCAGACCTC ACCTTAGTTC TGAATGAGAG 60 TTAGAGAGCC TGGACGGTGT CCCTAACACC AGATTATGAG AGGATAAGAG CCAGGACAGA 120 GCGGCCTCGG TGCCCGCCAG TGCAGAAGCG CTCCGGGAGC CGGGGAGGGA AGCCCGGGAA 180 GTTGCAGGGA TGGAGCTGCC TGAGCCTAGG GGAACATAGC TACTGTCCGC GGTGCTGAAA 240 GGGATCTCCT GTCGCCTTCG GGGCGCTGCC CATGGTGCTG ACGGCTGCGC CGGCCGTGTA 300 TGGCTCTGTC CATGGTTCTG AACCCACAGT CGGCTTCGGA GCTCTGTCCG CGGTTCTGAA 360 ATTCAGAGCC GCTTTGGAGC TCTGTCCGCG GTTCTGAAAT TAAGAGCCGA GAGGAGCCGA 420 CCCCGCTTTA GAAGTCGAGG GCTTGTGGGC TATGGAGATA CAGCAACAGG TTCCCTGGCC 480
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