Tag | Content |
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EnhancerAtlas ID | HS050-44579 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr22:30129070-30130210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE41 | MA0636.1 | chr22:30129076-30129086 | GTCACGTGAC | + | 6.02 | BHLHE41 | MA0636.1 | chr22:30129076-30129086 | GTCACGTGAC | - | 6.02 | MITF | MA0620.2 | chr22:30129072-30129090 | GTCAGTCACGTGACCAAG | + | 6.34 | MITF | MA0620.2 | chr22:30129072-30129090 | GTCAGTCACGTGACCAAG | - | 6.34 | USF1 | MA0093.2 | chr22:30129076-30129087 | GTCACGTGACC | + | 6.14 | USF2 | MA0526.2 | chr22:30129074-30129090 | CAGTCACGTGACCAAG | - | 6.5 | USF2 | MA0526.2 | chr22:30129072-30129088 | GTCAGTCACGTGACCA | + | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_65901 | chr22:30128976-30130779 | Pancreatic_islets | SE_66883 | chr22:30127747-30132023 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 30129528 | 30129628 | chr22 | 30129200 | 30129400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I029733 | chr22 | 30129149 | 30130450 |
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Enhancer Sequence | GAGTCAGTCA CGTGACCAAG TGACACCCTC GGGATGAGGC CTGAGGGCCT GGAATACCAG 60 CCCCACATCG GCTGCAGACA CGGCCTTCCC ACTTCAGCTC CCTCTGCTCT GGCACACTCC 120 CACACCCCAA CATCCAGCCT TCAGGCAAGG TGAGGCCCTG GCAGCTCCTG GCAGGCTCAG 180 GGGCCCAGTG GCCAGCCCTC TGCAGAGAGA GAAGGGCTTG GGCCTGCGGA GAGGGGTTTG 240 GAGAGGCCTC TGACCTCCGA GGGGGAGGTG GAGAGCCGGG GTCAGGAGCC CTGGGAGTTT 300 CCCCTGCTGC ACCCACCCAA CCTGCCCCTC TCTGGACCAG ACCTGCCATG CAGAGTCAAG 360 GACTCCGGGG AGCTCTGGGT GCAGCCTCCA GGACCCCCAG GTGTGAGAGG ACAGGGACAT 420 CCCCTGCTTC ATGGCTCACT GCCTGCTAGA AAGTGCAGAA GGCAGCTCTT GACATGATTT 480 ATGGCACTGG GGAGATTTCA TAAACTCCAC CAGCCGCAGA GAAGGCGGGG AGGCTCCGCA 540 GTTGCTGGAA GGGAGTGCCC TAGCTGCCAG CCAAGCCTGG GCTCCCTGCA GGGCCACAGG 600 GACAGTGGGG ATCCCCAGGG AGGGTGTGAT CCTGGGGAGC CCCTTCCCCT GAGCCTCAGG 660 CCCTTCCTCT AGAAAATGGG GCAGATTCCT GGGAACCTGG GACCTCCTGG GTCCAAGTCT 720 CAGCCCCGTG CCCCTGCCTG CCCTGAGGTC CCGCCAGTAG ACAGGCATAC CCAGTGCCTG 780 CTCACACACA CTGGCACACT GCCAGGGCCC CAGACACGTG AGCCAAAGCC TTGGGGACAT 840 TGAGGTGCGT GTCTGGCACA ACTCTGCTCG TAGCTTCTCT GGTGACCTGT TTGTCCTGTG 900 CGTGAGGACA GGAGCCACTC TCTTGCATTT TCCCAGCCGC GGTCCTAATC AGAGGAAACA 960 GAGTCGAGGA GGAGGATGGG CCAGGATGGC AGCGCCCGCC CAGAGAGGGG TGCAAAGGAG 1020 AGATTAAGAG GGATAGAGTC GCAAACTGAA GAGCCAACAA TGGGCAGCAG GGCCAGGCCT 1080 GGCCTTGCCG AGGGATTAGT CTGTGTGTCT GAGGCCGCCG CTGCTCTTGA CAGATCCCTC 1140
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