Tag | Content |
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EnhancerAtlas ID | HS050-60960 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr6:168134290-168136840 |
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: 5 | Chromosome | Start | End |
chr6 | 168134351 | 168135412 | chr6 | 168135600 | 168136777 | chr6 | 168135695 | 168135858 | chr6 | 168135864 | 168136350 | chr6 | 168136390 | 168136695 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I167733 | chr6 | 168134254 | 168135592 |
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Enhancer Sequence | CTGAGTTCCT GTCTCTCCAA CTCTCACCTG AATTCCTGTC TCTCCATCAT CTCTCACCTG 60 AGTTCCTGTC TCTCCACCTC TCACCTGAGT TCCTGTCTCT CCACACCCTC ACCTGAGTTT 120 CCTGTGTCAC CTGTTGTAAC AGCCCTCTCT TAAGAGGTCA GCTGGTTAGG AAGCTCCAGT 180 GTGAAAACCG TCCATAGGCA TTGGTGGTTC ACGGGACATT TTCCTTGGCA GAAACTTCAG 240 TTTTACTGAG AACTGAGCTG GAAATGTACG TGTAAGCACA AGAGGCCTCC CAGAGCATTT 300 GACCCAAATC CAGCACCAGT GTTGCATCCT CTTGCTGTAA AATAGGACAT TTTTTCAAAA 360 GGAGTGTGAA GTAAGTATTG ATTCACAAAG TGCCCTGAAG TCCTTGGATA CTCCTGTCCC 420 TGAATTCCCT CCGTGGATTC CCCACCCCGT CTCTCAGTGT TTGGACAAGC GTGGGTTTTC 480 TGACCAAACA TTCTAAACAA TGGCCTAAAT TCATCCCTGA GAGGCTGGCA TTCAGCCTTC 540 TGTTTTCAAT CTTTTTGAAC TCAACTGTGT ACTTGGACTG AGATTTTACA TTGTGCAACT 600 TCCTGACAGT AACGTGCCAT TACCCTGGGG GGTAAAGGGC TATTTAAGTC CAGACTCAGC 660 CATTCCCACC AGCCACAACA GAGCCAGACC TCTCCGTGCC CCGGGAGGGT GCCCTGAACT 720 CAAAATGTCC CTTGGCGATT GGGTTTAATA ACAGCATTTT CAAAGGCACT CCCCAGTCCA 780 CCATGGAATG TGGAGGCTGC CTCCTCTCCT GCCTCCGCTT TGCGGCACAG CTGTGGCTCT 840 GGGTCCCACA TGACTGCACA AAGTCAATGC CAAGGGCGTG ACCAGGGTGC CCGAGACCTC 900 ACTGTGGTCT GGGTGGAGCC CCAGCACTCA GGGTGCAGCT GCGCAAAGAT TGCAGGCGCC 960 TCTCCTGGGG CCTGAGCTTG TAAGTGTCCT TTGGATGTTG GGATGGGACA CCTGACTCCT 1020 CAGTAGGGCA CAAGGGGCCA CTGTAGGAAT AAAACTCAGA AAATCCCCCT GTTCACACTC 1080 AGCAACAGCC AAGCCCCCTT CAGTGTGATG CTGTGGGTGC TGACCTACAA ATCCTCACCC 1140 AGACACCTGC CACCCCGGAC CCCACAGAAT GGGCAGGACG AAGATCCTCC TGGTTTGGGG 1200 CGAGGAAGTG ACACCCTGGT CCCAGGACAT CTCCAGGGTC CTCTGTCAGA TACACACCCT 1260 CACCAAGCTG GCAAATAGGA TGTGTCCCCA TTTCACAGAT GAGGAAAGTG GAGCCCAGAG 1320 AGCTTCCACG ACTTTCCCAG GGTTGCAACA GAGCGAGGAG GGTCAAAAGG AGGATGGAAT 1380 GGGCATGGCC CCCAGCCCGT CCTTGACCAC CAGTTCCTTC CTCTGTCTCC AGTTCCAAAG 1440 GGGTCATCAC AGAGCACTTT GAAACCCCAG GGCTTCCCCC ACCGACCTCC CCCACTGACC 1500 TCCGCCGCTG ACTTCCCCTG CTGACCTCTG CCACTGACCT CCCCCTCTGA CCTCTGCCGC 1560 TGACCTCCAC CGCTGACCTC CCCCGCTGAC CTTCCGCCGA CCTCTGCCGC TGACCTCCCC 1620 CTCTGACCTC CGCCATTGAC CTTCCCTGCT GACCTCCACC GCAGACCTCC CCCGCTGACC 1680 TCTGCCGCTG ACGTCCCCCA CTGACCTCCC CCTCTGACCT CCGCCACTGA CCTCCGCAGC 1740 TGACATCCCC CGCTGACCTC CCCCGCTGAC CTCCGCCACT GACCTCTGCC ACTGAACTCC 1800 ACTGCTGACC TCCCCCACTG GCCTCTGCCG CTGACCTCTG CCGCTGCCCT CCCCCGCTGA 1860 CCTCCCCCGC TGACCTCCCC CACTGACCTC TGCTGCTGAC CTCTGCTGCT GCCCTCCCCC 1920 GCTGACCTTC CCCACTGACC TCCCCCACTG ACCTCTGCCA CTGACCTCTG CTGCTGACCT 1980 CCCCTGCTGA CCTCTGCTGC TGACTTCTGC CACTGACCTC TGCCGCTGAC CTCTGCTGCT 2040 GACCTCCCCC GCTGACCTCC CCCACTGACC TCTGCCATTG ATCTCCCCCG CTGGCCTCTA 2100 CCACTGACCT CTGCCACTGA CCTCCCCTGC TGAACTCTGC TCCCTCTATT TGTCCAGCTC 2160 CAGCTGCTCA AGAGACCCTG CAACCCTGAG GCCACCCCCT CTCCGTCAAC CCCATGGACA 2220 AAGTGAGCTC CTTCCCCAGC TAGAGAGGCC TGCACCCCCA CCTGGCTTCG TGTCTGCTTT 2280 CTTATGTGTT TTTGTTTACT TTTCTCTCCT CAGTCTTTCT CGTGGATATT ATTCATATTC 2340 CTTAACTCCG TTTCTAGTCC CTAAGACACT CTGGAAACAT ATTATCCTTG CCTGAAAGAT 2400 TCCACTCATA ATAAAGTGCC TTGCACTGAA TGTGCTGTTA GAATCACAGG AAAACAGGTG 2460 TCACTGGAAG CTGCCCTGCC GGCCGGAATC CTGGAATAGG GCAACACCTG GAATGGGCCT 2520 TTGTTGGCTC CAGAGAATAG AAGCTGGTGG 2550
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