Tag | Content |
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EnhancerAtlas ID | HS091-36118 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:1305950-1307600 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr4:1306711-1306726 | GGAGGGCAGGGGTCA | + | 6.26 | NR2C2 | MA0504.1 | chr4:1306718-1306733 | AGGGGTCAGAGGTGA | + | 6.9 |
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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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Enhancer Sequence | TTGGTCCCGC CTGGCGGTCC CTCTTCAGTC TGGGGCATGG ACACCCCTTT TGTCTCGAAA 60 ATGAGTCCTA AGACAGGCAA GCTGCAATGA TGGGAACGCG GGAGGTGCGG TTGGGGGCCC 120 CCTTCCCTGC TGTCTGCCTT CTGGGGCCAC TGTCGGCTGA GCAGGCCAGC TTCCTGTTCC 180 TGTAGGGACC GTGTTGTCTT GCTCCAGGAG TGTCCAGAGT CCAGGCCACA GGGAGACCAG 240 GATGTATAGC AGGTTGATTG ATTTTTTTTT TTTTTTTTTT TTTTTGAGAC AGAGTCCCAC 300 TGTGTCATTC AGGCTGGAGT TCAGTGGTGC GATCTCAGCT CACTGCAGCC TCCACCTCCG 360 GGGTTCAGGC GATTCTCCTG CCTCAGCCTC ACGAGTAGCT GGGACTACAG GCGCCCACCA 420 CCACGCCCGT CTAATTTTTG TATTGTTAGT AGAGACAGGG TTTCACCATG TTAGCCAGGC 480 TGGTCTCGAA CTCCTGACCT CAGGTGATTC ACCTGCCTTG GCCTCCCAAA GCTGAAATTA 540 CAGGTGTAAG CCACTGCACG CGGCCTGATC GATTATTTTT AGATGGAATT TCACCTCCAA 600 GGAGCATGTG GAGTTCCTTG TCACTGGGAT TGGTGGACAG GGGCCTTGGG ACTAATCTGG 660 CCCACTGAAG ACACCCAGAA AGTGGGATGA GATATCTTGA AACGTCGCAC TGAAAATACC 720 CAATAAACCA TGAAACCGAA AGGAATCGCC AGGCCAGAAC CGGAGGGCAG GGGTCAGAGG 780 TGAGCAGCAA GAGACTGCTG TTGTCCCCTG GAGTGTTGGC CAGGCCAGAT GGAGGTGAGG 840 ACCGATGACC CAAGCCTTGG AAAGTGGGGC CCAGTGGAGA GAAGGTGGGA CCCCACGGTA 900 CTACAGCTCA GCGTGGGGTG TACCAGAAGT GGACTGGCGT TGACACAGCA TTGCAGCCTA 960 CGTTCAGAGG ACTGGGATGA TTGGAGACCC TCAGCCTTCA CTCCGGTGAG GTGGTCCCGG 1020 CTGGTGGTGC CTTCCAGCTC CGGGCAGAGT CAATTCAGAT TCTTTCTTGG GGAGGATACC 1080 TTCAATATGG GCATAAGATG ATTCTTAGAT TCTCAGTTTT CAAGTACAAC GTCCAGCACA 1140 GAGACAGCCT GGGCAACAGT GAGACCCTGT CTCAAGACAC CACGATGGAC TGGAGACCCA 1200 GCAGGCAGTA GACAGAGGGC TGCACGGACT GCAGGTGCAG GGGCTGCCAG GTGCCACACC 1260 TTACTGTGCT TAAAGAACAG AAGCAGGCTG GGCGCGGTGG CTCACACCTG GAAAGCACTG 1320 TGGAAAGCTG AGGCAGCAGA ATCACTTGAG CGCAGGAGTT TGAGACCAGC CTGGGCAGCA 1380 CAGGGAGACC CCATCTCCAC AAAACATTAA AAATAGCCAA GCGTACTGGT GCCCTCCTGT 1440 AGCCCCAGCA GATACTCAGG AGGCTGAGGC AGAAGGATTG CTTGAGCCCA GGAGGTCAAG 1500 GCTGCAGTGA GCCACGATCA TGCCACTGCA CTCTAGCTGG GCGACAGCGA GACCCTATCT 1560 CAAAAAAAAG TTTGAAAGTC TCTGCAGGGA ACAGACAGTA TAAAAAGTGA TTTAAGGCTG 1620 GACACTGTGG CTCACTTTGG AAGGGCGAGG 1650
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