Tag | Content |
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EnhancerAtlas ID | HS050-01873 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:40391920-40392830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:40391988-40392009 | CCTCTCTCACACTCATCCTCC | - | 6.09 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34178 | chr1:40392146-40392833 | HCC1954 |
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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 |
GH01I039925 | chr1 | 40391365 | 40393731 |
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Enhancer Sequence | CTGGGGTGGC CCCACTTCTG CAACGGCCTC TTGCCTCCCT GACACCTGGA TGTCTTTCTA 60 GCCTTCACCC TCTCTCACAC TCATCCTCCA AATCATCACC AAGTCCTGTC AGCCCTCCCC 120 TTCTACAGAT CTTGCGTCTG TCCCCTTCCC TCTACCCCTG GCTCACTCGC CCAGCTTGTG 180 CTTCATGGTC TCCTGCCCTG GCTATGACGT CAGCTTCCTC CTTGGTCTCC CTGCCTGCCA 240 GTTCTCCCAC CTCCACCCTG CCCCATCTCT CCTCCACATC AGCAGCCAGA GGGCCCTTCT 300 AAAACACAAG TCTGACCTTC TTAGTGCCTG CTAATGATAT CCCATTGTTC TCTGGCTAAA 360 GTTCAACTTC CCGCACAGGT CACCAGGTTC TGTGGGCTCT TGTCACTGAC CTCAGCAGCC 420 TCATGCTGAC TGCTCTGCTG GCCTGCTGTG CACTCTCACC AAACAGAATG CTGACTCTCC 480 CTCCTGGGAA CAGGCCCTGG GCTGGGCCTT CTTGCCTCTG GGCCTTCGTT CCCATCACCG 540 ACCCTGCCCA CCACAGTCTC TCTCACCCAT CTCTGATGAC TGAAGTTCTG GCCACCCTTC 600 AAAGCCCAGC TTCATGGAGT GCCTTTTGGC CAGAGCTCGG TGTGCCTTGG ATTAAAGTTC 660 TTTGCGTTCC TCTCTCTCTC CCCTACTGAG CAGTTTGAGC TCCTGTGTGT CCCTTCTTCT 720 GTGCCCGGCG TGGTACCTGA TATGCTGAGG AGTTCTGAGA GTGTGTGGAG GGGGCACCTG 780 AGCCTCTGTC TCCCGTCCCC TTCATCTCTG GCTCCTTGCC CTAATCTGGA TCTGTTCCAG 840 CAGCAGCAGC AGTTCCAGGT TTGGCTCCTG GCTCAGCATC AACTTCGATT CTAGCTCTGA 900 CCTGCCTCAA 910
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