Tag | Content |
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EnhancerAtlas ID | HS091-24749 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:55915850-55918180 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:55916362-55916377 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 | AGTGGAGGGA GGGGTACAGG GTCAGGGCAC TCAGGAGTCC CAAGGCACCT CAACACCCCA 60 AAGTCCAGTC TCCACGGTCT GATTGTGATG CAGGTGGGTG CCCCGCCAAC TCTGCCAACA 120 GACTGGAGGA TTCTTTTTTT CTTTTTTTGA AATAAGGTCT CTTGTGTCAC CCAGGCTGGA 180 GTGCAGTGGC ACAATCTCAG TTCACTGCCG CCTGCAATTC CTGGGCTCAG GTGATCCCAT 240 CTCAGCCTGC CAAGTAGCTG GGATTACGGG CATGCCACCA GGTCTGGCTA CTTTTTTATT 300 TTAAGAGATA GGGTCTCACT ATGTTGCCCA AGCTGGTCTT GCACTCCTAG GCTCAAGCAA 360 TTTGTTCACC TCAGCCTCCC AAAGTGCTGG GATTACAGGC GTGAACCACC ATGCCCAGTC 420 AGGCTGTAGA ATTCTTAAGA GCAAGAGGCC AGGTGTGGTG GCTCACGCCT GTAATCCCAG 480 CACTTTGGGA GGCTAAGGCG GGTGGATCAC CTGAGGTCAG GAGTTCAAGA CCAGCCAGAC 540 CAACATGGAG AAACCCCGTC TCTACTAAAA ATACAATATT AGCCAGGCGT GGTGGTGCAT 600 GCCTGTAATC CCAGCTACTC GGAAGGCTGA GGCAGAAGAA TCCCTTGAAC CCGGGATGGG 660 GAGGTTGCAG TGTGCGGAGA TCGCGCCACT GCACTCCAGC CTGGGCAACA AGAGCGAAAC 720 TCTGTTTCCA AAAAAAAAAA AAAAAAGCCA AGCGCGGTGC CTCACACCTG TAATCCCAGC 780 ACTTTGGGAG GCTGAGGCGG GCGGATCACA AGGTCAGGAG TTCGAGACCA GCCTGGCCAA 840 CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAAATTA GCTGGGCATG GTGGTGCACG 900 TCTGTAATCC CAGCTACTTG GGAGGCTGAG GCAGGAGAAC TGCTTGAACC CAGGAGGCAG 960 AGGTTGCAGT GAGCAGAGAT TGTGCTATTG CACTCCAGCC TAGGCGACAG AGCAAGACTC 1020 CGTTTAGAGA GAGAAAAAAA AAAGAGCAAG AATGGCTGGG TTCCTAGGGG GCCACAGGAC 1080 CTCCCCCAAA ACCTCAGAGA TGATGCCCAT CTTGCAGCCC CCACCTGTGT CACTATCAAG 1140 CTCGTCTGCA CCCTCCTGGA TCCCCCGTCT CAGCCCAACT GACCACTCCA GTCACAGGCC 1200 CTTCCCAGGT GGCAGGGACC CAAGTACGCA CTTTCCTATA AGATGCCCAT TTATATGCCT 1260 TTCAGATCAA GGATCCAACT GTCTGTTAAT TCCACAGCCT CCCAACCCAG TGAACGCCTC 1320 TCCCACTCAC CCACTTGCTT GGGTCAAAAT ACTGTCCCTC CCCTAGCCCA TCAGCAGCCT 1380 GAGCACCGGC CTGCTAGGTC CTCCCCTGAA TCTCATCCCA TCTCCAAGGC TAGCTTCCTG 1440 GCTGGCCTCT GGGTTCTTCC CCCTGCCAGG CCGGCTCTCC TCACTACAGT CAATAGGAAC 1500 TTTGGAGGGA TTTGTCACAC CCCTGCTTTA AACCTTCCAC CAGCTTCCTC TACAAACTCC 1560 TTGAAGAGGC CTAGAAGCCC TAAAAGAGCT TGGCAGCTTC ATCATCAACT TTCTTCATGT 1620 GTTTTTACCA AGCGCCCAGC TCCACCTGCC CAAGGGCCTT TCTGGAGCCT TCCTATTGTC 1680 ATGATCCCGC GCCCTCTGCA GCAAGGCATG AAGGACCTCA ACTGTCACCG CTGCCAGGTC 1740 TTTCCTGACC ACCTACCACC ATCACCACCG TGGACTAGAC CATTCCTTCA CAGGCTCTGC 1800 TCAAATCCTG ACTTTGTAGG AATTCTGGTG ATAACAGAAA TGTAGCCTGC ATGAAACAGT 1860 ATTCTAAATC ACTCCGCAAA TCATGTGACC CGCAAATCAT TCATGACCCG TCTCCCCACG 1920 ATCTGCATCT GGCTTGTTTC CTCATCCCTG ACACTCACAG CAGGATGGAG TTTGAGATCA 1980 CCTGGCCCAC CCTCCCAGGC CCTTGCTGAC ACCATTCCCA CCACCTGGAG CTCTCTTCCC 2040 ATTCCTACTT AATTCCTACC CACCCTCAGG TCCAGGGAAG CCATGTCTGA AAGCCTTGCT 2100 TCAAATCTAG AGTACCGTCC CATGATATAC TAACTCAATG ACCAGATATT TCTCAACCCT 2160 TGTGGGAAAA GAGTACATAA TTGTCATTTG TGGCGTCCTG CCCTGTCCAC CAATGCATCC 2220 CAACACCTGA CACGAGGCCA GCCTGTAATG GGTACTTCCC GCTAGGGTGA TCTAGAGCAG 2280 GGTGATGGAG GATCTAAGCA GCAGCCCCTT CTCTTTTTCC TTCCAAACTC 2330
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