| Tag | Content |
|---|
EnhancerAtlas ID | HS047-31959 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:150595240-150596220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr7:150595736-150595755 | CGACCACCAGGTGGCGCAC | + | 7.5 | | JUN(var.2) | MA0489.1 | chr7:150595383-150595397 | GTGAGTCATCTCCC | - | 6.02 | | ZNF263 | MA0528.1 | chr7:150596106-150596127 | GATGGAGGAGGGGACAGAGAA | + | 6.15 | | ZNF263 | MA0528.1 | chr7:150596109-150596130 | GGAGGAGGGGACAGAGAAGGG | + | 6.96 |
|
| | 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 |
| GH07I150897 | chr7 | 150594219 | 150596117 |
|
Enhancer Sequence | TACCCGCAGT CAGCAAAAGG AAGTGTTAAT AAGCTCGCCC ACATAAACCC ACTTTGCCCA 60
CTGCTCAAAC CACCGCAAAC CAATTTTTCC AGGCTGCTGC CAGGTTAGGC TCCCTTGGTG 120
TTAATTTCCT GCTCAGTAAA GCAGTGAGTC ATCTCCCTCC CTTCTCTCCA GCTCTCACTA 180
TTGCTCTGAG ACCAGAGTCT GCAGCAGAGG GGTCACATGG AATCCTTTAG TACAGAAGTT 240
CACGACCTGG ACGAGGAGAC GCAGGGACCG CCAACTGGCT CCTTGGAAAC TGCCCGCAGT 300
TGATTCCGAA AACACACCTG AGCCGAGAAG CTCCATGCAA TCTGGAATTC CTGGAGTTCT 360
TGTCAGCGTC CACTGCCATG CAGGACTCTG GGGCACTTGG CTTGTCATTG GCTAAAAGAT 420
GGGCTGGGTT CGAGGTGCAG ATAGCTGCAT TTTAGCCGCT GGTGCTGTCT CGCTTGGAGG 480
AATGCTGTCT GCCACGCGAC CACCAGGTGG CGCACAACAC CTCGCGGCGA CTGGACCGGG 540
CACGGCTGCC TCTTATTAAT CCCGCGGAGA AAACAGAGGC TGGAAATGCC CCCGGGGTGA 600
GGCTTGACCA AGAACGGCAG ACTCAAAATG GCTCCCTGTG GACCAAGTTC AGCTGAATGG 660
AACAGAAAAA TGTGTTCACA GCGGCTTCAA CAAGAGACAG TCGTGTTTCT CTGTAAACAC 720
AGTCCTGAGT GGCTTAGGGG CCCCATGAAG GCCTAGGGCA CGCAGCCTCC TTCCTCCTCA 780
CGGCCTCCAC CTGGGATGTA GCCCCCAGCC TCCTAGTCCA CGGTGACTGC CAGAGCTCCA 840
GCCATCTCAT ACAAGTCAGG CAGTAGGATG GAGGAGGGGA CAGAGAAGGG TATGGCTACC 900
TTCACTGTGC TTTGCCGGAA TTCACAGACA TCACTTGTCT TACAACTCAT TGGCCAAGCC 960
TTAGCCATGG AGGCTGGGGG 980
|
