Tag | Content |
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EnhancerAtlas ID | HS101-01001 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:31319430-31321750 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr1:31320725-31320739 | CAGGTCATAGGTCA | + | 6.56 | Rxra | MA0512.2 | chr1:31320725-31320739 | CAGGTCATAGGTCA | + | 6.06 |
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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 |
GH01I030846 | chr1 | 31319734 | 31321163 |
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Enhancer Sequence | GAGAAGCATA CCCCAAAGCC ATTGGGCACC CTCCTCGCTC CACTCAGCCG TCTTCCACCT 60 GTGGCTTGTT CCTCAGTTTC ACGGCTTCCT CCTCAGATTC GTGGCCTCAG GACCACAAAG 120 TGGCTGCTCT GGGGCCAGCA TCTTGCCTGC GTTCTGGGCA GGAGGAAGGG GACTGGCAAG 180 GAGCCAAAAG CCTATAATAC CCCTGGGTGG CCTCCAGACT TTCCTGAAGA CACACTCAGT 240 GAACCTGCTC AGATTTCATG GGCTAGAATG TGTCATGTGG CATCCCAATA AACCAGGGAG 300 AAGGGGAAAA AAAACAGTTT TGGTCTTTTA GTCTGGGCGC CTTTTGCCAC CATGAAGAAA 360 GTCTGGGCTC TGTGAGTAAA AATGAAGAGG GTGGCAAGCA ACTGGGTCCA CCCCAGGGGG 420 CCTGAGGCCA GCCCCAGCCT GCCATTAACC TGTTGTGTGG TTTGAGGCAT GTCCCTTCCC 480 CTCTCTAGCC TCAATTTCCC CATTTCAAAA TGGGAGAACT GGGCCAGATG CTATGGGACT 540 TTATTCAGCT TTGACTGGCT GGTGCAAATC CTGACGCTGC TACCTATGAG CTGTGTGACC 600 TGGGGCGGCT ATTGGACAAA CCTTTGGCTC AGTTTCCTCA TCTGTAAAAT AGGGGTAATC 660 GTGGAGCTGC CTCATAGGGT TCTGAGGACT GGATGGGCTG TTACTTGTAG GGCGTTCAGC 720 AGAGTCTGAC AGGAAGGCAC AGACAAAAGC CATCAGTGAC GCTGTTATGC TAAGCTCTGA 780 GAGTCCACGA GTCCTGAGTC CTGCTTCTGC GCGCCTCTGT GTGCTGGGTG ACCTGAGGCA 840 GGTGCCTTCC CCTCTTGGGG CCCAGCAGGT CTGAGAGTTG CCTTCAGAAG CTGGGCCTGG 900 CTGTGACAAG AGAGTGAGTC CCTTCCTGGG CTGGGAGGGG GAACAGGAGC GGACGGAGTC 960 AGCCGGTTTC CTGCAGCCGG GGCAGTGACC TGGGCAGCAG GGACTTCCTG TTTCCCAGAG 1020 GGAATCCGGG CCACTGCATC CAGCCCCTCC CTCCCCTCCC TGCAGCTCCC CTCTGTAATG 1080 GAGGAAACTT GTCGCTGGGG CAACCTTCCC TGCGTCATCT CCCGGGGCGG GCGGCCCTGT 1140 GTGGGTGAGA GAAGCACCAG CAACAATCGC CCTTTGTCTC CAGCTCAGCT GCTCCCAAAG 1200 CGCTTTCTGA CCTTGCCCTC GTCTCAGCCC TGAGAGTCTC ATGCCCATTT TCCAGATGAG 1260 GAAACTGTGG CCCAAGGAGG TGAGGTGACT TGCCCCAGGT CATAGGTCAC AAGGCTGGTG 1320 AGAAGTAAGG CTGGGATTAA AACCTGAGTC TTCTGAAAAC ATGGGCCAGC TTCATCTGGG 1380 GCCCTCGGCA CCCAGTGGAC CCTCAGTCAG GGCCCCCGAG ACACTGTCAG AGCCTGGAGC 1440 TTGACTTTTC AGTGCCCTGA TGACCTAGGA TGTGATCCTC GGCCACTGTC GCCTCCCCAG 1500 CTGGAGCCCT GAGGAAGGAG GCTTGGGGTC TCCTGCAGGA CCCCTTTGTC TTTAACATGC 1560 ACACACCATC CGGCTTCGTG ACACTTGTCC CTGGGGACAC AGAGACCAGC CAGACCCACT 1620 CTGCAAAACC TGGGCACAAA CAACTTTAAC TCAAGGTGGC CAGTCTGACA TGCCACTGGC 1680 TAGGAGCAGA GGCTTTGCAT CCCCGGGTGC AAATCCTGAC CTTGGTACTT GCCGGCTGTG 1740 TGCCTTAGGC TAGTGACTTA ACCTCTCTGA GCTTCTGTTT CCTCGTCTAT GAAATAGAGG 1800 TCATGTTAGT TCCCTAGTGC TGCCATAAAC AAACTGCCAC AAACTTGTTG GCTTAAGACA 1860 ACAGATATTC AATCTCTCCT AGTTCTGGGG ACCAAAAGTC TGAAAACAAG ATTTTTGGCA 1920 GGGTTGGTTC CTGCCATGAT TTTTGGCAGG GTTTGCTCTG GGGGAAAATG ATGTGGATGA 1980 TTCTCTCCTA GCTTCTGGTG GTGGCCAGAG ATCCTTGATG TTCCTTGGTT TGTGGCTGCA 2040 TAACTCCCAT CTCTGCCCCC GTCTTTGTCT TCCCTCTGTG TAGGTGTGTA TCCAAATGTC 2100 CCTCTTCTTA TAAGGACATT GGTCAGTGGA TTAGAGCCCA CTACAATCCA CTGTGACTTC 2160 GTTTTGACCT GATTACATCT GCAAAGACCC TATTTCCAAA TAAGGCCACA TTCACAGGTA 2220 CAGGGGTTAG AATGTGAGCT TGTTTTTCTG GGGGACACAA TTAGACCCAC AACACTGTTA 2280 TGGGTTGTGG TGCAGATCTT ACAAGTAATT CATCTAAACC 2320
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