Tag | Content |
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EnhancerAtlas ID | HS050-69681 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:104243790-104244820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr9:104244593-104244603 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr9:104244593-104244603 | GGCACGTGCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 104243988 | 104244122 | chr9 | 104244132 | 104244325 |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I101478 | chr9 | 104240578 | 104244329 | GH09I101482 | chr9 | 104244647 | 104244820 |
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Enhancer Sequence | CTTTGCATGT GCTCTTTGAA ACACAACCCT TCCCTAAACA GAATTCTCTA CCTGTTACCA 60 TATCTAGAGT GTAGGGCTCA GGGAAGACAG TAAAGGACAC AGACTCTGAG AAATGAACAT 120 GAACTAGGGC TTAGATGAAT AAATGGAGCT ACAACAATAG TTATATTTTA GTGCAACTTC 180 TGAAAATTAA ACTAAAGGAT CCACGGGTGT GGAAGACACA ATACCAGGGT GTGAGTCAGG 240 GGATGAGTGC TCAAGAATGT TCTGTGTTTC CCAAATCCAC TATATGAATG GCACGACCAC 300 TTTCCCAGGC AACTCAGTCT AAAACACTAG TTAGTTCTAA CTTCTCACCT CCACGCAGTC 360 ACTTCCTAAT CCCACCTCTA CGGCCTCTTT TATTATGCCT CTCTTTTCCC CTCGCCTTCC 420 CCTTGTCAAG CTTTCCTCCC TGCCACACTC TAGTTCCTCC TCAGCACCTC CAAGCCAGCT 480 GATTGCAACA GGCTCCTAAC AGAGCTTCTG ACCTCCAGAA TGAGCAACAC AAGCCAAAAG 540 ATCTAGGTCC AATTCTCGTC CCAACACTCA CTAATTTGAT CAATTTGTAT AAAAAAATCA 600 TTTATCTCTC TGAGCCTATT TTATTTCTCT GTGAAACAGG AAAATAAAAG ATACTTCAAC 660 CAGGCGCGGT GGCTCACACC GGTAATCCCA CCACTTTGGG ACGCCGAGGC AGGCGGATCA 720 CGAGGTCAGG AGATCGAGAC CATCCTGGCA AACATGGTGA AACGCCATCT CTACTAAAAA 780 TACAATAATT AGCTGGGTGT GGTGGCACGT GCCTGTAATC CCAGCTACTC AGGAGGCTGA 840 GGCAGGAGAA TCGCTTGAAC CAGGTAGTCG GAGGTTGCAG TGAGCCAGAT TATGCCACTG 900 CACTCCAGCC TGGCAACACA GTGAGACTGT GACGATGAAG AGACAACAGC TATGATAGCC 960 CTTTGTCAGG CATAGGACAC TGTGCAAATG ATGGTGATGT TTTACTTGAT CAGCATCCAT 1020 CTGATACTCT 1030
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