| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13130 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:17886660-17887140 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr17:17886969-17886986 | AGGGACACAATGTTCCT | - | 6.36 | | Ar | MA0007.3 | chr17:17886969-17886986 | AGGGACACAATGTTCCT | + | 6.46 | | NR3C1 | MA0113.3 | chr17:17886969-17886986 | AGGGACACAATGTTCCT | - | 6.51 | | NR3C1 | MA0113.3 | chr17:17886969-17886986 | AGGGACACAATGTTCCT | + | 6.79 | | NR3C2 | MA0727.1 | chr17:17886969-17886986 | AGGGACACAATGTTCCT | - | 6.37 | | NR3C2 | MA0727.1 | chr17:17886969-17886986 | AGGGACACAATGTTCCT | + | 6.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26812 | chr17:17885681-17887641 | Esophagus |
|
| | 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 |
| GH17I017982 | chr17 | 17886077 | 17887277 |
|
Enhancer Sequence | TCAAAAAACA TTGCCAAACA GTGCTCCAAA AAGGCTGAAT GAGGCAATCA ACCCTCCTAC 60
CAACAGAGAC ACATGTTTTC ATTCTATTTA TCACACTGTG GAAGGAAGGC CTCTGTCTGT 120
GTCCTGTGTC CTAAGGTGGA CCAGCCTCCT GGAGAGTCCC TGGCCTGGCC CCAGAAACAG 180
CACAAGCGAG TCTCCTGCCC AGCCAGGTCC AGCTCACTTC CACCCCAGCA ACTTTTTAGC 240
TCCACCCTAG TAAACCTATT AGGTCTTTCT GTGGCTCTGG GTGGCAGTAC CGATCCCCGC 300
CCACCTCATA GGGACACAAT GTTCCTCGAT GCTCAGCCGA CATCTCCAGG GTGCCTGCGT 360
ACTCCAGGGC AGGGCAGAAG AGTTCTAGGT CCCTTTTGTG TGGTTCTGCC TCACTCCTCC 420
TGTACACTAG CACAAAACTC TGACCCTAAC CTGAGACTGA AATCACCTTC CATTATTTCA 480
|
