Tag | Content |
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EnhancerAtlas ID | HS158-50694 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr6:168134250-168136610 |
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) |
FOXP2 | MA0593.1 | chr6:168136580-168136591 | TTTGTTTACTT | - | 6.62 | TEAD1 | MA0090.2 | chr6:168135072-168135082 | ATGGAATGTG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 168134351 | 168135412 | chr6 | 168135695 | 168135858 | chr6 | 168135864 | 168136350 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I167733 | chr6 | 168134254 | 168135592 |
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Enhancer Sequence | CTCCACCTCT CGCCTGAGTT CCTGTCTCTC CAACTCTCAC CTGAGTTCCT GTCTCTCCAA 60 CTCTCACCTG AATTCCTGTC TCTCCATCAT CTCTCACCTG AGTTCCTGTC TCTCCACCTC 120 TCACCTGAGT TCCTGTCTCT CCACACCCTC ACCTGAGTTT CCTGTGTCAC CTGTTGTAAC 180 AGCCCTCTCT TAAGAGGTCA GCTGGTTAGG AAGCTCCAGT GTGAAAACCG TCCATAGGCA 240 TTGGTGGTTC ACGGGACATT TTCCTTGGCA GAAACTTCAG TTTTACTGAG AACTGAGCTG 300 GAAATGTACG TGTAAGCACA AGAGGCCTCC CAGAGCATTT GACCCAAATC CAGCACCAGT 360 GTTGCATCCT CTTGCTGTAA AATAGGACAT TTTTTCAAAA GGAGTGTGAA GTAAGTATTG 420 ATTCACAAAG TGCCCTGAAG TCCTTGGATA CTCCTGTCCC TGAATTCCCT CCGTGGATTC 480 CCCACCCCGT CTCTCAGTGT TTGGACAAGC GTGGGTTTTC TGACCAAACA TTCTAAACAA 540 TGGCCTAAAT TCATCCCTGA GAGGCTGGCA TTCAGCCTTC TGTTTTCAAT CTTTTTGAAC 600 TCAACTGTGT ACTTGGACTG AGATTTTACA TTGTGCAACT TCCTGACAGT AACGTGCCAT 660 TACCCTGGGG GGTAAAGGGC TATTTAAGTC CAGACTCAGC CATTCCCACC AGCCACAACA 720 GAGCCAGACC TCTCCGTGCC CCGGGAGGGT GCCCTGAACT CAAAATGTCC CTTGGCGATT 780 GGGTTTAATA ACAGCATTTT CAAAGGCACT CCCCAGTCCA CCATGGAATG TGGAGGCTGC 840 CTCCTCTCCT GCCTCCGCTT TGCGGCACAG CTGTGGCTCT GGGTCCCACA TGACTGCACA 900 AAGTCAATGC CAAGGGCGTG ACCAGGGTGC CCGAGACCTC ACTGTGGTCT GGGTGGAGCC 960 CCAGCACTCA GGGTGCAGCT GCGCAAAGAT TGCAGGCGCC TCTCCTGGGG CCTGAGCTTG 1020 TAAGTGTCCT TTGGATGTTG GGATGGGACA CCTGACTCCT CAGTAGGGCA CAAGGGGCCA 1080 CTGTAGGAAT AAAACTCAGA AAATCCCCCT GTTCACACTC AGCAACAGCC AAGCCCCCTT 1140 CAGTGTGATG CTGTGGGTGC TGACCTACAA ATCCTCACCC AGACACCTGC CACCCCGGAC 1200 CCCACAGAAT GGGCAGGACG AAGATCCTCC TGGTTTGGGG CGAGGAAGTG ACACCCTGGT 1260 CCCAGGACAT CTCCAGGGTC CTCTGTCAGA TACACACCCT CACCAAGCTG GCAAATAGGA 1320 TGTGTCCCCA TTTCACAGAT GAGGAAAGTG GAGCCCAGAG AGCTTCCACG ACTTTCCCAG 1380 GGTTGCAACA GAGCGAGGAG GGTCAAAAGG AGGATGGAAT GGGCATGGCC CCCAGCCCGT 1440 CCTTGACCAC CAGTTCCTTC CTCTGTCTCC AGTTCCAAAG GGGTCATCAC AGAGCACTTT 1500 GAAACCCCAG GGCTTCCCCC ACCGACCTCC CCCACTGACC TCCGCCGCTG ACTTCCCCTG 1560 CTGACCTCTG CCACTGACCT CCCCCTCTGA CCTCTGCCGC TGACCTCCAC CGCTGACCTC 1620 CCCCGCTGAC CTTCCGCCGA CCTCTGCCGC TGACCTCCCC CTCTGACCTC CGCCATTGAC 1680 CTTCCCTGCT GACCTCCACC GCAGACCTCC CCCGCTGACC TCTGCCGCTG ACGTCCCCCA 1740 CTGACCTCCC CCTCTGACCT CCGCCACTGA CCTCCGCAGC TGACATCCCC CGCTGACCTC 1800 CCCCGCTGAC CTCCGCCACT GACCTCTGCC ACTGAACTCC ACTGCTGACC TCCCCCACTG 1860 GCCTCTGCCG CTGACCTCTG CCGCTGCCCT CCCCCGCTGA CCTCCCCCGC TGACCTCCCC 1920 CACTGACCTC TGCTGCTGAC CTCTGCTGCT GCCCTCCCCC GCTGACCTTC CCCACTGACC 1980 TCCCCCACTG ACCTCTGCCA CTGACCTCTG CTGCTGACCT CCCCTGCTGA CCTCTGCTGC 2040 TGACTTCTGC CACTGACCTC TGCCGCTGAC CTCTGCTGCT GACCTCCCCC GCTGACCTCC 2100 CCCACTGACC TCTGCCATTG ATCTCCCCCG CTGGCCTCTA CCACTGACCT CTGCCACTGA 2160 CCTCCCCTGC TGAACTCTGC TCCCTCTATT TGTCCAGCTC CAGCTGCTCA AGAGACCCTG 2220 CAACCCTGAG GCCACCCCCT CTCCGTCAAC CCCATGGACA AAGTGAGCTC CTTCCCCAGC 2280 TAGAGAGGCC TGCACCCCCA CCTGGCTTCG TGTCTGCTTT CTTATGTGTT TTTGTTTACT 2340 TTTCTCTCCT CAGTCTTTCT 2360
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