Tag | Content |
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EnhancerAtlas ID | HS050-44188 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr22:22271140-22272500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr22:22271154-22271175 | GGAGCAGGGGTGTGGGGAGGA | + | 6.81 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_47859 | chr22:22271602-22272212 | Pancreas | SE_47859 | chr22:22272222-22272663 | Pancreas | SE_68995 | chr22:22271442-22272747 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I021916 | chr22 | 22271101 | 22272310 |
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Enhancer Sequence | CTGGGAGCTT CAGAGGAGCA GGGGTGTGGG GAGGAGGACA TGGATGCTTG AGTAGGTGTG 60 GTGGGCGGCC CAGGGCCTGG TCCCAGCTCT TGCATCCGGG GCTAGTTCCC CTGCTTCCCT 120 AAGGATGCCC CCTCTGTGAC ACAGTGGACA CAGATAAAGC TGTCTTTTGG CTAGGCGCGG 180 TTGCTCACGC CTGTAATCCC AGTACTTTGG GAGGCTGAGG CGGGTGGATC ACAAGGTCAA 240 GAAATCAAGA CCATCCTGGC CAACATGGTG AAACCCTATC TCTACACAAA AATTAGCTGG 300 GCGTGGTGGT GTGCACCCGT AGTCCCAGCT ACTCAGAAGG CTAAGGCAGG GGAATCGCTT 360 GAACCCAGGA GGTGGAGGTT GTAGTGAGCC AAGATCGCAC CACTGCACTC CAGCCTGGAG 420 ACAGAACAAG ACTTCTCTCA AAAAAAAAAA AAAAGCTGCT TTTCTGGCGC TGGTCCTGGA 480 GAGTTGGAGG CTGCAGCCCT GGGCAGCAGG CACTGCCGGG AGCCGGGGGA GGGGACTGAG 540 AGCTCTCTCA GGTGGCTTGG GAAGGACCAG GAGAAAATGC ACAGACAAGG CTACAGACAG 600 GAGAGAGGAG GCCTGCAGGC AAAGTGGGAG TGGGGAAGGC ACCGGGCTCA GGCAGCCCTA 660 GGACAGCTGC TCCCATGCGC CCACAAGCCT GAGGGCCTCC CCCACATTCT ACGGAGAAGT 720 TCAGGGCAGC ACTTTTGGCC GTGGCTGGGC AGTGTCTGCG GGGAGGCATT TCTGATGTTT 780 GTGTGCCCTT GAAGCCTGAG CTCAGCCAGG AGCACAAGGG CGAGTTTCCC GGCCCCTGCT 840 GCCTTGCTTT CTCTTGATTG AGAAAGGAAC CAAAGATCAA AAGGCAGTGA AGAATTGGGG 900 ACTCTGAGAA GGGTGACTTT CCAAGGCTTG GACCCCTTAG CAGCTTTGCG GCCTAGGGGC 960 ACTTGACCCC TGTGTGATAA GCCGAATCCT CTTTGTCTTA GGTGGGGAAT TGGTAGCTGG 1020 CTCATCCCTT GCCCCAGCAC CTGCAGCAGC GTGGCAAACA CTTGGCCAAC ATGCGCTGAA 1080 GGACTGGTCG ACAGAGTCCC ACGACTGGCT GCTTCAATAC TGACCCCCTG AGGGCACTGA 1140 GAAGGCTCTG AAGCCGTCTC CAAGAGCAGT TTCATGTGTG CTAGGAGCTG CAGCCACATG 1200 GGACTGGGCC TGTGCGTGCT ATCCTGGGGC TTCAGGGGGA ACCAGCCCTC CAGCCTGCTA 1260 AGCGACCAGC AGCAACGCTC GGGCCAAGGC CCTGCATTTT GCTGCTGGCC GTCCTTGGGT 1320 GGGTGAGGCT ACAGAGGTCT GGACTGGAGG TTGTGGTTGG 1360
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