Tag | Content |
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EnhancerAtlas ID | HS091-38603 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:79963070-79965600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr5:79964311-79964326 | AGTGTCCAAAGTCCA | + | 6.18 | NFYB | MA0502.1 | chr5:79964052-79964067 | CTGATTGGTTCATGG | - | 6.92 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 79964166 | 79964596 | chr5 | 79963294 | 79963390 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I080667 | chr5 | 79963672 | 79964863 |
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Enhancer Sequence | GTTGATTAAC TTTTATACTA CATAGTATAT ACCTGCATTT AATATAGAAT ACATACTATA 60 TTCCATGACA TAAAAGTCAT GGAAACAAAA TAGGAAACTC ATCAAAATTA AAAGCAAAGG 120 CATTCTTAGG TATAGGAAAA TTGTTATGCA ATCCTTGGGG TGTTGCTTCG CCAGCTGTAA 180 ACCTCTGTGG CTGGTGGTGC CTTTGCCCGA GTTTTTACTT GGGCCTGCTG GGCTCATTCC 240 TCCCACTCGG CCTGGCAGGC TGTGCTTGGC TTTTGCTTTT GGCCTGAATC TCGCAGCTGC 300 CAAGGGTGAG CCAGGAGTGG AGTGGTGAGG GTGAGGGGTG TGTGAGCAGG TGACCATGGG 360 GTCTGGCCCC TGTGCACTGC CAGGCATGCT GGCTTCGGCA GGGTGGGCAG CTCCAGGTGC 420 CAGCGTGAGT GAGGGCTGGA CCAGGCGTAC CACAAACAGC TTCCACAGCT GGCACCAGGG 480 AACACAGTGG CGCCCAGAAG CTTGGAGATT CCAGGAACTG CAGAGCCCCA GAGAGGGTGT 540 CATAGACCTG GCTTAGGAGC CCCTAGGTCT GAGCTCCCCA GAGGTCCACA GCTCTTCTCT 600 CCTGTCTTCT CTCCTTCTTG TTGCTGCAAT GTGGCAAGCA AGAGATGGGT TTCAGGCCTG 660 TTTGTGTTAC AGCTCTTTTA GCCCTGCCAT TCGGTGGGTC CCAGGTTCTT GTCCTGCTTC 720 CAGGAAGAAT GAAGTATGTG GACGAGTGGA GGGTGAGCAA GGCAAAGAGG GGCTTCCTTG 780 AGTGACAGAA CATTGAGGGG AGACCCGCAG TGGGTGCTTC TTTCTGCAGG CAGGGCATCC 840 CATCAAGTGA GAAGTGATGA GCCTTCAGCC GAGAGGGGAC CCTGGAGTGG GTAGCTCCTC 900 TCCGCAGGCA GGTTGTCTGC TTGTCTCTTC AAGTTTGGCC GAGTCTGGGG ATTTGTATGG 960 GCTTGAGAGG AGGAAGTGTG TGCTGATTGG TTCATGGGCT GCCATGGGCG GGCTCAGAAA 1020 ACACCGTAAG TTCTAATTCT GGTTCGTCAG CCTGGCCCCC AGGCTTCAGG CTGTTCCTGG 1080 CTTGAAGGTG GGGCTTCACC CGGACCTGAC CCTTTCTGCT CAGGAGCCTG TCTGCCTCCT 1140 GCCGTCATCC ATGGCACCCA GGCTGTTTGT GCCATGGGGC ACCTGCAGGA CAGCTCTGAG 1200 CTGCCCTCAG CCCTCTCCTT GGCCTCCTTC CCATGTTCAT CAGTGTCCAA AGTCCAGAGG 1260 GGGCCGAGGC AGCAGGGGGC TGGCATGTTA GCACTGCCCT GAGCATGTGC ACACCCAGCC 1320 AGGTTGCAAC AGTTCCTAGG CTTGGCCTTA ACTTTGAGAT CAGAGTGGGT GCTGGGAGCT 1380 GGGAGAGGCC AGGCAGTCGG AGCAGGTACT TCTGAGCCTG CAGAGGGAGG GGGAATTCCC 1440 TTTCTGGGCC CTTGAGATTG CAGAGATGCC CGGGTCCACA GCCACAGCTT GGGTGGCTGT 1500 GGCTGCAGCT GCACCCAGGA GGGTGGGGCT CCTGCCTGCT CCCAGCCCCC AAGAGCACAG 1560 GGATGCCCAG GTTTGCAGCC ACAACTGGGC AGCCACAGCT GTGCCCAGGG AGCGTGAGGC 1620 TCTCACCCTG CCAACTCAGA AGGGGGCGAG GCTTCTTCCA CCCATTTCTG GCTCCTGTCG 1680 GTTCTGTGGA GCATGCAGCC CTGGCTGCGC CTCTCCTACT GCAGCTGGCG TTACGGCAGT 1740 GGCTGCTCCA GATGGGCTGC CATTGCCATC ATAATGACCT GGATTTCTCT TGCCAACCTC 1800 TCCATGCCTC ACCGTCTTCT TATTGCTGAT CTTTGGAGGT TTGCTGGACT GCACTGTTCA 1860 AATAAATTGA GTTTTTTTTG AAAAGTTAGT ATCTTTACCT GATGTCCCGG TGAAGCTGAA 1920 TTGTTTTAAA CATTTGGGAA CTACAAAGTG TACATGTTTC TGGGTTTTCT TTTGGATTGG 1980 GGTTCCCATT TCTGGGCCAT TTTGCTTCTC TCTCACTCTC CCCTCTTCTT TTTGGTCACT 2040 AGATTTTTAG GCCATATTTT TCATTGTAGG GGGAGCTGGG TAAATTTTTA GAAGTTGGCA 2100 GTGACAGAGT GGCAATTAAT TAGAAGTTGG ATTTAGCCAA CTATAAATTT GTCTCATTTA 2160 CATTTTTCTA AATTAAGTCT AATAAGCGAG GAATTTTCCC TAAGCTGTGA ATTGGAATTA 2220 ATTATGGTTC CTCACAGAAA GGTAAGAATA GTAGGAGTAC TAATGTTGAA AATGTGGCCT 2280 TGTGCTGTAA ATTTTTTAAC AGCTCTTTCT CATGTTTCTT TACCAAGAGA ATCATGGTTC 2340 TTTCTTTCTA TAAGAATTTA TAGAATGTGC TGTCTTTTAC AGTGTGCTTG GAAGTATAAA 2400 ACATTAAGTG CAGCTTTATC TGTTGGCATG CTTTGCTCAA AGTGGTTTTG CCCTACTCCT 2460 GAGAGAGAGC CAGATTTGTC CCCATTGGCC TTTTGTGCAT TACACACCTT AGAATAAATA 2520 ATAAAAAGAA 2530
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