| Tag | Content |
|---|
EnhancerAtlas ID | HS184-29171 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr8:37683670-37684920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:37684340-37684361 | CCCCCACCCCTGACCTCCTCC | - | 6.07 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_27453 | chr8:37683176-37684684 | Esophagus | | SE_27924 | chr8:37683009-37684426 | Fetal_Intestine | | SE_28818 | chr8:37682918-37684483 | Fetal_Intestine_Large | | SE_46699 | chr8:37683869-37684423 | Ovary | | SE_54469 | chr8:37683058-37684474 | Spleen | | SE_68481 | chr8:37637808-37685395 | TC71 | | SE_68482 | chr8:37637808-37685395 | TC71 |
|
| | 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 |
| GH08I037825 | chr8 | 37683090 | 37685994 |
|
Enhancer Sequence | AGCCCCTTGG CAGCCCATGA AGGGAAGTGA CACAATGAGG AATGTGTTTC CCTCTGCCCG 60
TCCCCCACGT GGGGGTGGGA GGCTGAGCCC TGAGAATGGC CAGACCCCAA CAGGGGCCAG 120
GGGGCACATG CTGGGACAGT CCCAGAGGGG CAGGCAGTGA GGATGGGGTC TGGCGGCAAA 180
ACGGTGGGGG CTGGGCCAGA GGGGCACCCC TGGCAGCCAG GATACTTATC CTGCATCCCT 240
CTCCCTCGGC CAGGGGCCTA GGATCAGTGT CCTGGCACGG TCCCTGTGTG CGCCTCACTG 300
GGGGGCACCT CCCAGCACAC CCCAGCATGG AAGCCATCCC TCCTCTAGGG AACTGGCCCC 360
TTCTGGTGGC CCCTTCCCTT CCTTCTCCAG GGACTTGGGG TCATGGAGGC CGGCTGAGTC 420
CTTCGAGTCC TTCCTATGGG AAGGAGCTGA GGGTGAGGGC TCCCCTGGCC GTGGGAAGGG 480
CTGTGCACAG TGTTTCTGTC CCCAAGCGGG ACTGTGCACA AACAGGCCCC CTGGTGGGAC 540
AGTACCTCCC CGTCCTGAAC ACCCATTTCC TCTCCTCCCA GCGGGCAGCC GGCTTGGTTA 600
ACCCCCTCCT GCCCAGTAAT CCAGAGACGT TGATGAGGTT GTGGTGGGCA GGGCCAAGAG 660
CCTCCTCAGC CCCCCACCCC TGACCTCCTC CTCCATCTGG GCTGAGGGGT GGCAGGGCCA 720
AGAGTCCCCT CAGCCCCCAA CCCTGACCCC CTCCTCCATC TGGGCTGAGG GGTGGTAAGG 780
CCTGGGAAAG CAAGTGGGCC CCAGAAATCT CTGTGGATCT CCTGTCTTCC CGCCACAGCC 840
CCTTCAGACA GGGGGCCCCC ACCCTTGCCT GCTCCAGGGG TCCACCCACC CTTGCCTGCT 900
GCCTCACAAT CTCCTGCCAG TGGGTGGGAG CCAAGAGGCC ACTGCCTCCA TCTCAGACCC 960
AGCACAGGGA GGCCCACTGG GCTGTGAGGC CCATGAGCTC TATGGAGCCT GAAGCCTGTC 1020
CTGGTTTAGC TCAGGAAAGA GCCAGCTGGC CTTTGAGTAG GTGGGCAACT GGCCCCACCC 1080
ACTCTGCCTT CTAGGCATCT GTCCCTGGCT GTGCAGGGCA CAGAGGACAG GGTGAGGGAG 1140
AAGGCCAGTG AGCAGGCACC CACCTTGGTC TTCTGTGGTC CTGCCTGCCC CAAGAGCCCA 1200
GGGGGCTGCC CTGGCAGGTG TGGGGTTAGG GCAGGCAGAT ACCCAGCAGG 1250
|
