| Tag | Content |
|---|
EnhancerAtlas ID | HS047-04847 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:105492220-105493410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr10:105493048-105493059 | AGGAGATAAGA | - | 6.14 | | HNF1A | MA0046.2 | chr10:105492255-105492270 | TGTTAAAAATTAACA | + | 6.05 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26541 | chr10:105491044-105493294 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 105492437 | 105493261 | | chr10 | 105492597 | 105492760 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I103732 | chr10 | 105492210 | 105493405 |
|
Enhancer Sequence | ATTTTCCGTG ATTCCCATCC AATCTGCTGC TTATATGTTA AAAATTAACA CTGATATTGG 60
GCTGTGAAAC CGCCATTAGG TGGTGGGACT GGCTGGCCAG CAAGGGCAGG GAGCCCAAAG 120
TCTGGGGAGG TCCACTGCAC GGTCAGACTT TCCATGTCTG AGTCCTTGCA GGGAGCCGGC 180
TGCTCTGTGT GCAGAGCCAG CTGCACAATT TTGGGTGCAT TTGAATTCCC ATCAAACCCC 240
AGACTCTGAG CCCACATTGT CTAGCAGGTC GAAGGAAGAT GACCAGCCAA GCAGGTGGGC 300
TATGCAGGGC ACTGTAAGTA GAGACTCCAG AGGCTCTAGG CAGTACGTAG ACAAAGGCAG 360
GTAGAGACAG GGGAAGGTCT GGCCGTGGAG CGGACTGCAC ACGGCACTGT GCTGGCTGGG 420
GTCGGCCGGT GATGCTGAGT GGTCTGTCTG GAGGCCAGCT GTGAAATGCA TAGCTAGGTG 480
GCAGTGGCCA TGGACTTGTC CCTAAAAACC ATTCCAAGGT CAGTGGGTTT CTCAGACAAT 540
CAGACCACAG ATCCCAGCTT CTTAGTTCAG CAGAATTAAA GGTCACTCTG TACTGCCCCA 600
CCCCCGCCAT TCTCAGAGTA AATCACCGCC TGTGAGATAG ATGGCTGTCT GCTTGGTGAG 660
CCCATGGCCC CATTCCTTGT CTGGCTCTGG GCAGTTTCCA TCTGTGCTAA TCAGGTTAGG 720
AGGTCCCTCC TCTTGCAGAC CCCACTTCAA TGGCTCCCCC AGCTACGCGT GGTACACTGG 780
AGCTCCAGAG CCCCTCTGAA TCAGGAGTCC TGTTCAAAGC CTGATCCCAG GAGATAAGAT 840
GCTATCACTT CCTCCTCCGG ATGACCCAGC AGACAGCATT TCCTTGGAGC CCAACTGCAG 900
ATGCCTTGGG CTGGCTAATC TGAGCTATAA ATCCCAGCTG GAAAAGCCTT CCTCCCGCCC 960
TATGCCCCCT CCTCCATTAG CTTTGCCCAT TTATTTAACT TCTTGAGAAA GGAAAAAAGA 1020
GAAATAAAAG CTCAGGCTAC AGCCATCAAT TTAACCAGAA ACAGTGAATG CCTGTTAAAG 1080
AGAAAAATGA ATATTGGTCT GAAGAAGAGA AGTTTCTAGC TTAAGGGAAT CCAGCACTGG 1140
GGCATCCTTT TAAAATAAGG CAGAACATGT GACCCAAGTA TAATGTTCAC 1190
|
