| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12072 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:11453020-11453880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr16:11453675-11453689 | ATGCCACGTCATGA | + | 6.34 | | FOXA1 | MA0148.4 | chr16:11453095-11453111 | TACTAAGTAAACAATA | + | 6.84 | | Foxa2 | MA0047.2 | chr16:11453096-11453108 | ACTAAGTAAACA | - | 6.44 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_39207 | chr16:11452904-11455078 | IMR90 | | SE_44615 | chr16:11452928-11459306 | NHDF-Ad | | SE_68391 | chr16:11438909-11459249 | TC32 |
|
| | 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 |
| GH16I011353 | chr16 | 11447820 | 11459775 |
|
Enhancer Sequence | TGCACTCCAG CCTGGGTGAC AGAACGAGAC TCCATCTCGG GGAAAAAAAA AAAAGTGAGC 60
CCTTTTACAG AAAACTACTA AGTAAACAAT AGTACAGTGG TACCTGAGTG ACTGATGTTT 120
GGGTACTTTT TCCTGATGTT CTAAAATAGA GCTGCACTGT CCAATGTGAT TGTCACCAGC 180
CTCATGGAGC TGTGGAGTAC TTGGAGTGTG CTGGTGTGAT AGACAGAGTG GCCAAACTTA 240
GTAAATAAAA GTGTAGGGTG CCTCCCATTC CACCAGTGTG GGCTGTGCAC AGTGACTTCC 300
TTCCAGAATG GAAAGGGGGA TGAAAGAGTA ACTTTACGGT GGTGAAACCT GACAAACTGC 360
CTCAGCCAGC TGGCCAAGGT TAACATCAAG TAATACATCA CGTTAATAGC ACACATGGGT 420
AAGATGCCTG AGGCCCTGGG AGGCCAGGAC TTAGAAGCCT CAAATTCCAC AGCCAGTCCT 480
CACCGCCCTC ACGTGGCTCC TGCAGAGAGT AGGGACAGTG CCCTAAGGGG ACTTTGGGAG 540
TCTCATGTGA CCACATGAGG TCTCTTGAAG GCCTGGAGAG GCATTTGCGG ACATGGTGTC 600
TTCCATAGGT ATGACAGCCG GGGTTGGTGC TTGAGACCTC TGGTCAGAGC CTGTAATGCC 660
ACGTCATGAA TTGCCACAAA CTTAGCAGCT TAAAAAAACA AATGTATTAA TATCTCACAG 720
TTTCTGTGGG TCGGGGTCTG GTAGGGTGTT GTTAGGTTCT CTGCTCAGGA CCTCTTCAGG 780
CCAAAATCAA GGTGTCAGCC AGCTGAGCTC TCTTCAGGAG GCTCTGGGAA GAATCCCGAA 840
TGGGCATCCA GGCTCATCAG 860
|
