| Tag | Content |
|---|
EnhancerAtlas ID | HS101-08076 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:66188940-66189590 |
Target genes | | Number: 45 | 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 | ATTCGGGACT CGGGAGATTC GGGACTTTCT ACTTTTCCTC CTGAGCTCCC TCCAGACCTC 60
ACCTTAGTTC TGAATGAGAG TTAGAGAGCC TGGACGGTGT CCCTAACACC AGATTATGAG 120
AGGATAAGAG CCAGGACAGA GCGGCCTCGG TGCCCGCCAG TGCAGAAGCG CTCCGGGAGC 180
CGGGGAGGGA AGCCCGGGAA GTTGCAGGGA TGGAGCTGCC TGAGCCTAGG GGAACATAGC 240
TACTGTCCGC GGTGCTGAAA GGGATCTCCT GTCGCCTTCG GGGCGCTGCC CATGGTGCTG 300
ACGGCTGCGC CGGCCGTGTA TGGCTCTGTC CATGGTTCTG AACCCACAGT CGGCTTCGGA 360
GCTCTGTCCG CGGTTCTGAA ATTCAGAGCC GCTTTGGAGC TCTGTCCGCG GTTCTGAAAT 420
TAAGAGCCGA GAGGAGCCGA CCCCGCTTTA GAAGTCGAGG GCTTGTGGGC TATGGAGATA 480
CAGCAACAGG TTCCCTGGCC AAGAGCTGCG GGCAGCGGGT CAACAGGTGT TTGCAGAGGC 540
AGGTCCATGA GAAATTCCTC TGGATTCTCT GAAACTCAGA CCATGCCTTC CTCACTTCTT 600
CTCTGCCTCC CAGTCTTACT CCTGACGCAC TACGTCTTCT CGCCCTACAG 650
|
