| Tag | Content |
|---|
EnhancerAtlas ID | HS195-07447 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr9:139290220-139291150 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr9:139290790-139290806 | TCCAAAGTAAACAAAA | + | 6.6 | | FOXP2 | MA0593.1 | chr9:139290794-139290805 | AAGTAAACAAA | + | 6.62 | | Foxa2 | MA0047.2 | chr9:139290791-139290803 | CCAAAGTAAACA | - | 6.74 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_42000 | chr9:139288672-139292472 | LNCaP |
|
| | 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 |
| GH09I136394 | chr9 | 139288673 | 139292472 |
|
Enhancer Sequence | TCCTGGTAAC GAGCCAGAAA TGGCATGTGA CGAGATGAGA CGTGGATGCT CCCCTGTCCT 60
CGGCAGCCAG TCGCCCATCG CTGGGCCTCT GGGACACCGA GGCAGCTCTG GCATAGCAAC 120
ACCCAATGTG GAAGCAGGAA GTGACCCTGG TGGGCAGCGG GAGGGCGTCT GAGTTTGGGA 180
GTGGAGCCTG TCACTCTCAA GGCGGCCTGT GTGCGCCTTT CCTAATCCAC GGCAGGCAGA 240
GCCTCCAACC TGGAACACGC CAGGGCTGCG GCTGCTGCAA GGCAGCAGGC AGCTTTCCAG 300
GACCACAGGC GTCCTGTGAA CCCTGAACTC TGTCCTGAGC CCCTGTCGTG TGCATCACCA 360
GCAAAGCACG GGGAGCAAGC CTGTGTGGGA GGAAAGTCTC TGCAGAGCCA GGAAGTGGAC 420
GCAGTGAAAA TGCCCACTGG GAGGTGAGGT GCCCACAGGC TACAGCAGGG TGCTCACTCA 480
CAGAAGGTGA ACCACACAGC CACGCAAACA TGAGGAAACT CAGTACCCAC TAACTTTGCA 540
GAAAAAGGAA GCAGCAAATC GCCAACGTTT TCCAAAGTAA ACAAAAGGCA GCTAATAAAA 600
TAATCACTGG CCTCACAGAG CAGTTGCCAG GTGCTGTTTG GGTGCTTGTG TATTTTTCTT 660
TTTTTTGAGA CAGGGTCTCA CTCCATCACC CAGGCTGGAG TGCAGTGGTG CAATCACAGC 720
TCACTGGAGC CTCGGCCTCC TGGGCTCAAG TGATCCTCCT GCCTCAGCCA CCCAAGTAGC 780
TGCGTCCACA GCCACGTGCC ACTGCACCAG CTAATTTCTG TATAGCTGCT CGTGTTAACT 840
GACTTGTGCT GTAAACGTCC CCGCTGCCCC ACAGGAATCT GAGGCACAGA GAGGCGAGCT 900
GTGAGGGGCA GGACGCAGGT GCACAACTCA 930
|
