Tag | Content |
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EnhancerAtlas ID | HS159-02794 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr18:8960380-8961840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr18:8960863-8960879 | AGGGTCAAAGTCTGGA | + | 6.07 | POU2F2 | MA0507.1 | chr18:8960620-8960633 | ATAATTTGCATAT | + | 6.44 |
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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 |
GH18I008960 | chr18 | 8960448 | 8962013 |
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Enhancer Sequence | GTATTTTTGG TAGAGACGGG GTTTCGCCAT GTTGCCCAGG CTGGTCTTGA ACTCCTGGCC 60 TAAAGTGATC CTCTTGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCAT 120 GCCTGGCCTG AGACTAGAAA TTATAAAGGA AAGTAAGGGG AACAAAAACC AGATTTGTGA 180 ACCCTTGATT TGTACTCAAT TTTTAGGGAG TATTTACAGA GCAGGGAGTA GAATTTGTGC 240 ATAATTTGCA TATGTTTGTG CAGAATTTGT ATTTGAGACA GGAACAGTAT GTGGGAAAAG 300 TTATTATGTC TGTTTTAACG CCTATTCCAG CATGAACATA TTTTAAAACC CATAGAAATA 360 CATTTTAAAA TCATAAATAA CAGCAACAAA TAAAGTCTTT TGATAGGTTT ATTTCCTTCA 420 TTTGCCAGAG TAATTACGGT AATTCCCAAA TGACCAATTT GAACAACGAA GCCTCTTGTT 480 AGTAGGGTCA AAGTCTGGAT CCGTTAACAG CGGCATTCCT GTCAAAATCT GATCTTTCCT 540 CTAAGTGCCC AAATAGCCTA GGTGTACTAG ATACCATTCT TCATGTCTCT AATACGTGCA 600 AACAGACCTG ACAACTATTT CAGAACCTAG AAAGGCCAGC CAAAAGTTAG TCATTAACTA 660 AGCAGGATAA ATCTTAATCA ACTGAATAAA TGCAAAGTAT GTAACATTTT AAGTAAAACA 720 AACAGGGTAG AGTTAACCAA GAGCCCTTAC GGGAGGAAAA AAATCATTAT TTCTTCCTTC 780 GGGTGAGGCA AAAACCGTTT CTTTAAACTT GAAATGCAAA GAGCATTCAT TTATATATTT 840 CAGGATTAGA TTCCGGTCTC AGACTGATAT GCATTTCTTA AATGTGTCTT ACATTTTCCC 900 TGTTGAGAAA GTGGGTGAAT CAGAACTGAC TCAGGCCAGA CACACCACAG GGAGAACAGG 960 TCAGCACTAG AGTGAGAATG TCTAGTATGC TACCTTTATT CTGTATTACT ATGATCCATG 1020 TCTATTTTGT GTTAATTATT GCTTGTCCAA AGGGACCACC AGAAAAATCT GTTGATCAAG 1080 CAAATCTAAG TATATTAGAC CTACAGCAGT AAGGGACAAT ACTACAGTGT CAGTCTTAGA 1140 AGTGTCTCAA AACAGAGAAA TTAGGAAAGG GTGTTGGAGG GTGTTATGGC CCAGATTATA 1200 TGATTTTAAG GCATGTCTTG CAAGGCAAGA AACGAGATTG GGCAAAATTA AGATATAATA 1260 GTCTTGAAGA GGTGAACACA AGAGGGTGAG GGTCTTTTGT TTTGGTTTGT TTTGAAACAG 1320 AGTCTCACTC TCTCACCTAG GCTGGAATAC AATGGTGCCA TCATAGCCCA CTGCAGCCTC 1380 GAACTCCTGG GCTCATGCTA TCTTTCTGCC TCTGTCTACT GAGTAGCTAG GATTACAGGT 1440 GTGGCACCAC AGCCAGCTAA 1460
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