Tag | Content |
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EnhancerAtlas ID | HS118-12061 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr22:29260140-29262200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr22:29261141-29261156 | GGTAAATCATTAACT | - | 6.71 | HNF1A | MA0046.2 | chr22:29261141-29261156 | GGTAAATCATTAACT | + | 6.82 | HNF1B | MA0153.2 | chr22:29261142-29261155 | GTAAATCATTAAC | - | 6.46 | HNF1B | MA0153.2 | chr22:29261142-29261155 | GTAAATCATTAAC | + | 6.82 | SPIC | MA0687.1 | chr22:29261598-29261612 | AGAAAGGGGAAGAA | + | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 29261088 | 29261244 | chr22 | 29261004 | 29261197 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I028865 | chr22 | 29261004 | 29261197 |
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Enhancer Sequence | AAAATGAAGT CAGTGATCTC CAGATGAGAT CCTCCTGGAT GACCTGGGTA GAGTCTACAT 60 CCAATGACAA CTGTCCTCAT AATAGACACA GGAGGAAAAG ACACAGAGCC AAGGGGAAAG 120 TCATGTGAAG ATGGAGGCAG AGATTGGAGT GAGGGAGCCA CAAGCCAAAG AACTCTGGCA 180 GCCACCAGAA GCTGAAAAAG ACAAGGAAGC ATCCTCTAGT CTTTGGAGGG AGGATGGCCC 240 TGGTGACACC TTGATTTAGG ACTTATGGCC TCCGGAACTG TGAAACAGAG ACAGGGTCTC 300 CTTATGTTGT GCAGGCTGAT CTCGAAGTCC TGGGCTCAAG TGATCCTCCT GTCTTGGCCT 360 CCCAAAGTGC TGGGATTACA GGTGTGAGCC TCTGTGCCTG GCCTCATTTC TGTTGTTTTA 420 AGCCACCAAG TTTGTGGTAA TTTGCTACAG CAGCCCTGGG AAAATACTAA TAGGCAGGAA 480 GCTGGAGCGG GGAGCAGCAA AGTCAGGGGA CAGGGAGCCC AGACTAGAGG CTGGAGAAGA 540 CCAGGCATGT AGCAGGATGA GGCGTGCTCA CCTCCCACAC GCACCAGGAG CAGGGCAGTC 600 CTCTTACTCA TAGGCAGGTC CATTCCCCCA GGGCTAGGAG GATGGGGTCT CTACCTTCAC 660 TATTTTCTTT AGAAAGAAGA AAGAAAGAAG AAAGATAGTG ATGGCGGTAA GGACAACAGG 720 GCCCTCGGGG GCACATGGCT ATGCTGTGGC CTGGAGAGAG GCAGACTCTT CTCAGAGGAG 780 GCTAAGGGCC TCTGGCTAGA GCATGGCTAC AAGCAAGGTG GCTAACATGA AGAGACCATG 840 GTGCAGAGGC AGATGCCAGC AGGCTAAAGG ACAATTCTGG AATGGGGCAG TGGGAGGGGT 900 CCTGTGTCTT TGGGCTTCTT TGATCCCTGA GACACTTTGG ACGGGACAGA GCCTTGGCCA 960 CCAACGGGGT CATGTCTGTT TAAACAAAAT TTAACACAGG AGGTAAATCA TTAACTCACT 1020 GAAGAAACAA ACAGGAGTGC AGGCCATATC TCTAGCACCA GGATTCAAGA GCCACGGGGA 1080 TGTTAAGAAC TCCTGAATAT CAGAAGTGGC TGCCACTCAT GGCTTCTGTA AGTGAGTGAA 1140 AGCATTTGGT GAGCACCTTC TATAAGCAAG TCTTCGTGCC AGGTGCTGTG GGAACAGATG 1200 CATGAAGAGG CTCAGAGTCT GACCTGAGCT TGGAGCTGGG GGAATACGAG CTCACAGCCA 1260 TTGTGAGCAT GCCCATGCCT GTCTCCAGGC CCACCACGGC CCATCCATCA TCTCATGTAA 1320 TTCTCATGCC TCTGAGGTAG GGCAAGGATT GCCTGCATTT CATAGACAAG GAAACCCAAG 1380 CTCAGAGAGG GAGAGCAACT TGCCTCGGCC ACACAGCTTG TCAGTGGTGG AGAAAAATAA 1440 ACAGGAGCTG GCTTTTGCAG AAAGGGGAAG AAATTGTTAG GGTTCAAGGA TGTGTTTAGG 1500 AACTTAAGGG CAGGAAGCAC AACTTCCTGA AAGACAGGAG CCAGGTCCAG CAAAGCCATC 1560 AGGAGGCAAG GCAGCCACTG ACCCTGTCTG GGACCATAGA GTCTCCCAAT TCTACTTCTC 1620 ATGGAAGATT TATTTTATTC TTCCCTCTAT TTGAAGGTTA AGAGCAAGGG TTCTGGCATC 1680 TGATCTGGGT CCAGTCCTGG CTTCACCATT TATTACCTCT GTGATCTCAG GCAAGCCTAC 1740 TTCCCCACCT ACAAAACAGG GATACCACAG TCCCCAGGTA AGGATCACAG GAGAAAACAT 1800 GGGCAAAGCC ATTGGCACAG TGCCTGGCAC ATAATATATG CTCAATAAAA CCCAAGTTGC 1860 TATTATCATT TTACTAGTAG GAAACAGCCT CCCCAAGCCT CCCAGCTCCA CAAACACCCA 1920 TCAACTCACT AGCACCCTCC TTCTGACTTC TTCAGCCAGA AGAAGCAACT ATTGCAAGTT 1980 GGTATAGCAA CTATACCAAC TATAGCAAGG GAGAGAGGGA GGGTCATTTC ATTCAAACAC 2040 AGTTTCAGGT ATGTGTGGAC 2060
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