Tag | Content |
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EnhancerAtlas ID | HS158-51600 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr7:36988700-36990130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr7:36989067-36989078 | CCACACCCTCT | + | 6.02 | Klf1 | MA0493.1 | chr7:36989065-36989076 | GGCCACACCCT | + | 6.32 |
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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 |
GH07I036949 | chr7 | 36989206 | 36990006 |
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Enhancer Sequence | TCCACCCGCC TTGGCCTCCC AAACTGCTGG CATTACAAGC GTGAGCCACC ATGCCTGGCC 60 TGCTCACTCA CTCTTCAAAG ATCTCATAAC ACTTTTTTAC CCTATGGTAG AGGTACTTAC 120 TTCCATCTGC CTTGCATGAT GAGAGACCCT ATCACTGAAC TGGAAACGGC ACCACTTCTT 180 ATTCCACTGT GTTTCCCCCA CATTCCCTTG CCTTGTGCCT TGGCCACAAA TGGAGGATAT 240 AAATATCTGC TGATTTTCAC GGAGACTCAC ACAAGAGCTG AAAAGACAGG TGGGACTTCA 300 CGGAATTTTC TCATCTGGTT CCTTTGATGA CAGACCAGCT GAAGAGCCCC CTTCTCAATG 360 TGCATGGCCA CACCCTCTCT CGGTGGCAGA CATCAGACCA GGTTCTCTTG CTCTGTCCTC 420 TTCACTCGGT CTAGGCCAGG GTTCTTCAAC CTTGGCACTA CTGACATTTG GGCCAGATAA 480 TTCTATGTTG TGGAAGCCTG TCCTGTGCAT TACAGAATGT TTAGCAGCAT CTCTGGCCTC 540 TATTCACTAG GTGTCAGTGG CCCCCCACCC CCAACCAAAT GTGACAAAAC TATCTCCAGA 600 CATTGCCAAC TCCCCTCATC CCCATGGCAA ATCCTTCCTG TTCACTGTAG AATGTTTAGC 660 AGCATATCTC TGGCCTCTGC TCACTAGATA CCAGTGCCCT CCTCCACCAC CCCACCCAGA 720 TGTGACAAAC AAAACTATCT CCAGACATTG CGAAATCCCT CCTCCCATTT GAGAACTACT 780 GTGTGGCCTC ATGCCAATGA CACAGACAAT GCAAACATCT TTCCAAAGCA AATCCCCAAA 840 GTCCCGTGGC TAAGCTGGTT CTGCAAAATT AGCTTCTCAG ATTTAGGTTA TGGCTCTTTC 900 GGTTGGAGTT CCCTCGTGCT GTGTTCGCCC CCATGCTCCT ATACATCTCA TTTCCATTCT 960 CCCCTTCTCA CTCACCACTT TTTTTCAGCA TTTAAATCTA GAAGATACAG CTCCCTGTAT 1020 ATCCTAAACA GACACAGAAA ACAAGAAACA ATGTACTATG CAAGACCCAC CATCAACAAG 1080 GTGCCCGGGA CAGCTGGAGA TGAGCGACTC CTGACTGGGT GGATTGACTG GCATGCTCAT 1140 TATTAACATC TGTGAGAGAC AGAGGGAATG TTTCCTTCAG CCCTGTGAGC AAGACTCAGG 1200 AACTGAGCAG CCCACAGTAG CTTTTTATGT AACCAGCCCA CCTTCTCTGC AGGAGATGAG 1260 CAGAGTCAAA AGATCTGTTT TCCTTCCCAT TTCCTCCTGC AGTTCACTCT TCACAGTGGG 1320 TGACTGGGCA AAGGGTCACT CACCACCAAG CCACAGGTTT CTCCTATTTT CTCCTGGGCC 1380 CCTGGCCACT CCTATCTTCT GCTTCTGTCT TTGGTTCAAC CCCTTGGGCT 1430
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