| Tag | Content |
|---|
EnhancerAtlas ID | HS092-09520 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:66188830-66189590 |
Target genes | | Number: 49 | Name | Ensembl ID |
|
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 |
|
| | 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 |
|
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
|
