Tag | Content |
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EnhancerAtlas ID | HS091-11037 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:118575950-118577250 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:118576901-118576916 | 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 | CAGGTGAGAG GTGAGAAAGA CGAGAAGAGC AGGTCATGCA GAGATGAGTT ATCGGGTGTA 60 AGTCCCTTGC TGGACACAGA GAAGTAGACC TGGTTTGGGA TGCCCCCACC CATGCTTAAG 120 CCAGAGAGTG CCTTTCCTGC CCTTTTGCCC CCCTACAGCA GGTGTCTGTA ACTCACAGCC 180 GAGAGCCATA TCCACCTGTG GCCTGTTTTT ATACAGCCCC ATGAGCTAAG AATGGTTTTT 240 ACATTTTTAT TTAGTTATTT ATTTTTTATT TTTTTGAGAC AGAGTCTCAG TCACCCAGGC 300 TGGAGTGCAG TGGCATGATC TTGGCTCACT GCAACCTCCA CCTCCCAGGT TCAAGTGATT 360 CTCATGCCTC AGCTAACCGA GTAGCTGGAA TTACAAGCGC CCACCACCAT GCCTGGCTAA 420 TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCTTGTCCA GGCTGCTCTC GAACTCCTGA 480 CCTCAGGTGA TCTGCCCGCC TCAGTCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCACT 540 ATGCCCGGCC TGGTTTTCAC ATTTTTAAAT GATTGGTGAA AAATTGAAAG AAGAATAGTA 600 CTTTATGATG TGGAAATTAC ACAAAATTTA CCTGTCAGTG TCCATCAGTT AACGTTTTAT 660 TGGAGCAAAG CTATGTGTCA TCTGTGGCTG CTTTCATGCT GCCAAGGCCA AGTTGAATAG 720 TTGCAACAGA GACTGTGGCC CCCAAAGCTT AACAAATTTA TTCTCTGGCC TTTTAGTGGA 780 AAGTTTGCTG ACCTTTGCTC TAGAAAATGT CAGAGGGTGG GAGGGGCTGG GTCTGCTCTT 840 CTGCAAACAC ATGAGGTTCG TGCTGGCCTC TAAGAAAGTG AGGACTGGGC CGGGCGCGGT 900 GGCTCATGCC TGTAATTCCA GCACTTTGGG AGGCCGAGTC GGGGGGATCA CGAGGTCAGG 960 AGTTCAAGAC CAGTCTGGCC AACATGGTGA AACCCCGTCT CTACTAAAAA TACGAAAATT 1020 AGCCAGGCAT GATGGCAGGC GCCTGTAATC CCAGCTACTT GGGAGCCTGA GGCAGAGAAT 1080 TGCTTGAGCC CAGGAGGAGG AGCTTGCAGT GAGCCGAGAT CGTGCCACTG CATTCCAGCC 1140 TGGGTGACAG AGTGAGACTC TGTCTCAAAA AAAAAAAAAA AAGAAAGGAC TGTTGTTCGT 1200 GGCTGTGTTG TGGCAGCCAG CATGTTCTTG ATGCCCAGTT GCTGACTGTG CAGTGAATGT 1260 TCCCTGATCT CCTGTGGTGC TGACATCCCG TGTTTCTTCA 1300
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