Tag | Content |
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EnhancerAtlas ID | HS050-43975 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr21:47444730-47445820 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr21:47444883-47444898 | AGTTAATGATTAACT | - | 8.33 | HNF1A | MA0046.2 | chr21:47444883-47444898 | AGTTAATGATTAACT | + | 9.03 | HNF1B | MA0153.2 | chr21:47444884-47444897 | GTTAATGATTAAC | - | 7.52 | HNF1B | MA0153.2 | chr21:47444884-47444897 | GTTAATGATTAAC | + | 7.82 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_02356 | chr21:47444870-47445641 | Astrocytes | SE_26913 | chr21:47445100-47445677 | Esophagus | SE_44138 | chr21:47444825-47445920 | NHDF-Ad | SE_45632 | chr21:47444324-47446296 | Osteoblasts | SE_46629 | chr21:47445173-47445576 | Ovary |
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| 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 |
GH21I046024 | chr21 | 47444608 | 47446066 |
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Enhancer Sequence | GAAGAATAAT GATGGAAATG TTCTATATCT CGATATGAGC AGTGGTCACA CAGTGTAAAT 60 ATATCTAAAA TTTATTGAGC TATACAATTG AGATTTGGGC ATTTTGCCAT ATGTAAGTTA 120 TTCCTCAATT TTTTAAAAAA AGAAGACAAG GAAAGTTAAT GATTAACTTT GATTTTTTTA 180 TTTTTTATTG TGCTTTTAGT ACTCTACCAA TAATGAAAAG GCATTACGTC TGTTTGAAAA 240 ACAAAGTATA AGTGTTTAAA GCTCTAAATT ATAAGGTAAA CCTATTTGTG TTCACATGAA 300 AAAAATCCAT GACACACTTT GACTGGAAAA AGAAAGTAGC AGAATGCCAG ATACAGGAGA 360 GTTCTGCTTT ATATTAACAT GAGAAAGACT TTGTTCCCAT GAGAACAACA AGAGAAACTC 420 AAACAAAATT AAAATTGTAC TTTTCTAAAA GACTGGGGTG GGGGTCGTGG TCAGGCAGCA 480 GCATGAAGAA AGCCTTGAGA ACTGAATTCC AGAAAGAAAC AAGCATAGGC AAGAAAGAGA 540 GATGACAGCT CCCAGGCTTC CTACTGAGGT CTGAGGAGGA TCGGCCTGCT GTGGATAAGA 600 AACTTTATGG GGACAAAGTG CTGTCTGCTG AACTTTGGGT GGCAGTATGA ACTGATGGGA 660 CAAATTGGAG TCTAGAAAAG CCACAAAGGC AAGGATAGAG CACATAACCT GAGCAATTCA 720 CCTTCCCCAC TCCAAGTTTT GACATAAACA TAGCAGTGGA GGAAGGGTGG CTAAGCAGAA 780 ATAAACCATA AGATCTCATA CTTGCTGTGA TTAATGGATT CCACACCCCT GCCTGAGTTG 840 AAACTGCAAC CAGCCCCCTC TAAGACCAAA CACTGACAAG TCTGAAAAAC TCTATCTCAG 900 GAATTTGAAG TTGAGTAATC ACAGGTTAAA GCTGCAATTT TTTTTTTTCT CAAGGAGATT 960 CTAGGAGAAA GCTGAGTGAT TGGCTTCTCA CCCTCACTAC ATTCTGAGGA AAGGAAATGC 1020 ATGTCTAAGG AACCAAAACA AAAATGCTTC AATCTTCATT ATTCATTTAT ACACAATGTG 1080 CCAAACAACA 1090
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