| Tag | Content |
|---|
EnhancerAtlas ID | HS182-21681 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:95419760-95420760 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr9:95420467-95420478 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr9:95420467-95420478 | GGATGACTCAG | + | 6.14 | | RREB1 | MA0073.1 | chr9:95420099-95420119 | CCTCCACCCACCACCACCCC | + | 6.7 | | RREB1 | MA0073.1 | chr9:95420102-95420122 | CCACCCACCACCACCCCCCG | + | 7.23 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26671 | chr9:95416004-95420818 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCGGCCACTC CACACAGGAA GATCTGACAG GGGCCACAGA TGCCAGGCCT TGGGGGAGTC 60
AAGGTTAGGG TGGTTTGGGC TCTGCAGTCA CTGAATGCAG CAAAGAAGGG GACAGAGAAG 120
GCTGGAGGCA TGGACTTTGT TTCCATGGGA TGCGTTCCAC AAACCAAAAC CACCTAGGCC 180
TATTTCTCTT CAGCAGCTGA GGCAGAAACC GCAAGACAGT GGGGCCTTCC TATCCTCCGC 240
CTGCCTGCCT CGACCCCACA CCCACTGTGG CCCCACCAAC GGCAGCTTTC TCCCATGGCT 300
CTCTCCCCTC TTTCTACTGT GCCCACGCGG CAGCTGTCAC CTCCACCCAC CACCACCCCC 360
CGGCCTCCCT TTCTATGACC TCTACCTCAG ATGCTCCAAC CTGCCATGTC CCAGGAGCCC 420
TCAAGGGGCA GTGACTCACC AACCCCATAC CATTGCCCAA GCCAGCCTCC GCCTGCTCCC 480
ACAGTGGAAC AGCCACCATC CAGGAGCTCA CCCCCAGCTC AGCTGCATGT GTCCCCTCAC 540
AGGACCCACG CATCAGATGG GGAGCAGAGA AGGGCCCTGA ATGCAGGAAG CCTCCGCGAC 600
TCGGTATGCA CCCCAGGACC AACAGAGATT TGCACAGAAA GCTGCAACTC AGTGGTCAAA 660
AAAGAGAGGG CAATGCTTTT TCACGGGTGG TCCATGGCAT TTTGCTTGGA TGACTCAGAG 720
AAGAGAAACC TAACGACCCC CTCCCACCAC AATGTTTAAC ACAGACTGTC TACCACCACA 780
CTGGAGACTC TATTTTCATA GACACAATTC CACAGATGGG GAAACTGAGG CAGCAGGTGC 840
TATGGAACTC GGCAACGCAA AGCTTGCCTG ATCCTGGGGT CCTCGCCACA AGCAGGGCCC 900
TCTGAGCAGG ACCTACAGGC CAGGCCAGGG CAGCTCCTGG CTGAGCGCCA CATAGACTAC 960
CACAGTGACA CATGGGTTAA CGTGCTGGAC CCAGTCAGTT 1000
|
