Tag | Content |
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EnhancerAtlas ID | HS158-39767 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr3:122084170-122085020 |
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) |
HNF4G | MA0484.1 | chr3:122084555-122084570 | TGAACTTTGCTCTCC | - | 6.3 |
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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 |
GH03I122362 | chr3 | 122081592 | 122086178 |
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Enhancer Sequence | TCTACCACTT ACTAGCTTGT GGCTTTGGGG GTGTCAGTTA GTATCTCAAG TATCTCTGAG 60 TCTTTTTCCT CAGATAGAAA ATGAAGAGGT AGAGCTGTAC CATCTCCAAG AGCTCTCTCT 120 GATTCCATAA TCTTCATAGC AAACTTGAAA ATTGAAAAAA AAAATTCACA TTTCCTTATT 180 TGCTTATGTA CTACCCCATG GTTACCCCCA ACCCTATATG TTATCAAGCT AGAAAGCAAA 240 CCTCATGCAA CTCACTGATT GGTTTCTAAA CCCTCCTTGC AGTGGTCATC CTGGTGATTC 300 TATCTGGGCC CTAAAGACAC AAGGGCAGAT CTCAAGGCTG AGCAAATTGT GTGTCACAAT 360 CATTCCCAAA CACTCAGTAG AGTTTTGAAC TTTGCTCTCC ACTAATGAGT CACTCTGTTG 420 TTTGACTTGA TCTGCAAACA GTGACTTTTC AGTTTCCAAT TTAACAGCCT TTGCCCTGCA 480 GTTTCCTTTG TCAACACCTT CAAGGGCGTT GAAATACAAA CTCCAAAATT ACTAGACTTT 540 CACCAGTTTT ATATAAATTA TCTATATGCC GGCTGGACAC GGTGGCTCAT GCCTGTAATC 600 CCAGCACTTT GGGAAGCTGA GACGGGCAGA TCACAAGGTC AGGAGTTCGA GACCAGTCTG 660 GCCAACATGG TGAAACCCTG TCTCTACTAA AAATACAAAA AAAAATTAGC TGGACGTGGT 720 GGCAGGCACC TGTAACCCCA GCTACTAGGG AGGCTGAGGC AGGAGAATCT CTTGAACCTG 780 GGAGGCGGAA GTTTCAGTGA GCCAAGATTG CACCACTGCA CTCCAGCCCA GGCGATAGTG 840 CGAGACTCCA 850
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