| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31843 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:138019330-138020610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr9:138019771-138019792 | TCGTTGTTTCAGTTTCGCTTA | + | 6.39 | | IRF8 | MA0652.1 | chr9:138019775-138019789 | TGTTTCAGTTTCGC | - | 6.26 | | IRF9 | MA0653.1 | chr9:138019775-138019790 | TGTTTCAGTTTCGCT | - | 6.55 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_33529 | chr9:138017838-138032579 | H2171 | | SE_34902 | chr9:138017575-138030599 | HeLa | | SE_66989 | chr9:138017838-138032579 | H2171 |
|
| | 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 |
| GH09I135127 | chr9 | 138019326 | 138020206 |
|
Enhancer Sequence | GCTCCCACAG CCCTTTGCTC TGCCTCTGAG GCATTGTCAT CCCCACTCGG CAAGTAGAGA 60
CATCGCGGCC CGGAGAGACT AGTTAACACC TGCCCAAGTT AGCACGGTAA GGGAGAGATG 120
GGCCTGAGAC GGAACCCAAG TCCCCTGACA CCCAGCCTCA GGCTTTTTCC AAGAGCCATG 180
TTTGGGGAAA TTGGCGTGAT ATCGAGCAAC TGCCTTCGAA TGGGCCAAAG TTTTCAGAAT 240
TGCTGGGGGA CCGGAGCCCA CTCCTCCGGA GGCCGCTTTC TTCCTTCCCG AGTCAGACTC 300
AGGAGGCTGG GCTGTAGCAA CACTGGAGGT TCCAGCAGCT GACTCTGTGA AAAGAAACAG 360
CAATTTCCTT ATTGATCTTC TCCTTCCCGC TACAGTCTGG AAAATAAGGT CGCCAAGAAT 420
GATGTTGTTG CTGCGTGTCT CTCGTTGTTT CAGTTTCGCT TATTGAATTG TTATCCCTGG 480
AGGACCCCCA GCCTCACAGC CACTACTTCA CCCCCAAACA GCTTCCTGTT TCAAGGACAT 540
CAGTGGCTCA TCCAGATTCC ACGAAAAGTG CCTTCTCTGG CTAGTGCCCT CCAGCACTGA 600
CCCCTCCGCT GTCCCCAGCA CAGCACAGCC TGAAAGGTGG CCAGCTGTCC GTCCACCAGC 660
ATCGCGATTC CCCAGCTTCC AGCCTCCTCA CTTCTGTAAT TAGCAGGACG GGCCCTCCTA 720
TCAGCCCCCA GGCTGTTTGT CTCGCTCAGG CTGGCTCCTG TTGTCCCTGT TAAATTGGCT 780
GTGGCAGGCC ATAATAAAGA AGAAAAACTG GCTGCATCAG GTCACTCCAA GAAGCTGACA 840
TTAGCTCCAG AAGGGCTGGG AAAGGAGAGA TTCAATTAAA CTTTTACTGC GGCCCGTCGG 900
CTCCTGGCCT GGCCTGTGAA TTCTGGAGCT GGGCTGAGGT TTGGAGAAGA CTCACAGCCA 960
GAGGAGCTTC CCCGGGGTCC CTCCTACCAG GAGACTGTCA GTCTGCACTA GTCCCAGGCA 1020
GGCGGGGGGA GCGTGGCCCT GTGGGGTTAC CCTGCAGCCC AACTCTGCAG AAGGTTAATG 1080
ATCGCACAGC TCCATGCCAA AGGCTCAAAC CAGACACCCC AGCCTCAAGG GGCTCTGAGC 1140
CTACTGCAGA AGACAGAGAC AGGGACAGAC AATTCCAGAA GATGTTCCTG AGTCTCCAGT 1200
TCTTGGATAT GAAACCAGCA GCTAATTTAG CCCACTCAAG TGCAATAAAA TCACAGACAA 1260
ATGCGGCGGC CTCTTCGGGC 1280
|
