Tag | Content |
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EnhancerAtlas ID | HS091-10001 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:54041420-54044120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr12:54043001-54043016 | AGAGTCCAAAGGCCA | + | 7.58 | NFIL3 | MA0025.1 | chr12:54043682-54043693 | TTATGTAACAT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr12:54041659-54041674 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 54042797 | 54043102 | chr12 | 54042838 | 54043000 |
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Enhancer Sequence | AGTATCCCCC TGGCAAAAAA AAAAAATTTT TTTTTTTTTT GACAGAGTCT TGCTCTGTCG 60 CCCAGGCTGG AGTGCAGTGG CATGATCTCG GCTCACTGAA ACCTCTGCCT CCTGGGTTCA 120 AGTAATTCTC CCGTCTCAGT CTCCTGAGGA GCTGGGATTA CAGGTGGACA ACACCATGTC 180 CGACTAATTT TTGTATTTTC AGTAGAGACG GGGTTTCACC ATGTTGGCCA GGCTAATCTT 240 GAACTCCTGA CCTCAGGTGA TCTACCCATC TCAGCCTCTC AAAGTGCTGG GATTATAGGC 300 GTAAGCCACC AAACCCGGCC ACCCTAGAAA ATTTTGCTTC CAATTCCTGC AACCTTATGG 360 TTTGCTGGCC TAGAGGTCTT ACTTCCAAAG GAAAGAATGC TTTTGCTAGG AGACACAACA 420 ATGATTCTAC TGAAATAGAA GTTAAGACTG CTAGCTGTTC ACAGGACACC TGCCACATGG 480 ACTCCTCATG CCTCTGAATC AACAGCCAAA GAAGGGAATC ACTGTGCTGG TTGGGGTGAT 540 TGATCCCAAC TACCAAGGCG AAATTGGACT GTTACTGAAC ATTGAAGTTA AGGAATAGTA 600 TATCTAGAAT ACAGGAGATC TCTTAAAGTG TCTCTTAGTA TTACCATGCC TTGTAATTAA 660 GGTCAATGGC AAACTACAAC AACCCAATCC AGGAAGGATT ACTAATGGTT CAGACCATTC 720 AGGTATGAAG GTTTGGGTCA CTCTACCAGG TAAAGAAACA TGACCAGCTG AAGTGCTTTC 780 TGAAGTCAAA AGGAATGGGT ACTTGAAGAA GGTAGTTATC AATAACAGCT ACAACCACGT 840 AACCAGTTAC AGAAATGAGG ACTGTAATAA TGTTATGTGT ATTCCTCTTT ATTTTGTTAT 900 AAATATGCTT GTGTATGTAT ACACACACTC ACACACACAC ACACACCTCT CTCTCTTTAT 960 ATATGTATAT GTATTATATT AGTCAGGGTT CTCCAGAGGG ATAGAACCAA TAAGCCATAT 1020 GTATATATAA AAGAAGTTTA TTGGCTGGGC ACGGTGGCTC ACAACTGTAA TCCTAGCACT 1080 TTGGGAGGCC AAAGCGGGCA GATCACTTGA GATCAGGAGT TTGAAACCAG CCTGGACAAC 1140 ATGGTGAAAC CCCGTGTCTA CTAAAAATAC AAAAAAGTAG ACAGGCGTGG TGGCGGGCGC 1200 CTGTAATCCC AGCTACTTGG GAGGCTGAGG CAGGAGAGTT GCTTGAACCT GCGAGGTGGA 1260 GGTTGCAGTG AGCTGAGATC TGGGAGGTGG AGGTTGCAGT GAGCCGAGAT CGTGCCTCTG 1320 CACTCCAGCC TGGGCAACAG AGCTAGACTC TGCCTCAAAA AAAAAACAAA AAAAACAAAA 1380 AAAAAGTTTA TTAGGGAGAA TTGGCTCACA TGATCACAAG GCAAAGTCCC ACAATGGGCC 1440 ATCTGCCAGC TGGGGAAAGA GAAGCCGGTA GTGTGGCTCA GTCCAAGTCT GAAAGCCTCA 1500 AAACTAGGGA AGCCAACAGT GCAGCCCTCA GTCTGAGGCC AAAGGCCCGA GAGCCCCCGG 1560 GAGGCCGCTG GTGCAAGTCC CAGAGTCCAA AGGCCAAATA ACCTGCAGTC TGACATCCAA 1620 GGGCAGGAGG AGAGGAAGCA AGTGTCCAAC ATAGGAAGAG AGAGACAGCC AGAAGACTCA 1680 GCAAGAGGCT GGGCATGGTG GTTCATGCCT ATAATCCCAG CACTTTGGGA GGCTGAGGTG 1740 GGTGGATCAT TTGAGGTCAG GAGGCTGAGA CCAGCCTAGC CAAGATGGTG AAACCCTGTC 1800 TCTACTAAAA ACATACAAAA ATTAGCCGGG TGTGGTGGCA TGCACCTGTA GTCTCAGCTA 1860 CTGCGGAGAC TGAGGCAGGA GAATCGGTTG AACCCAGGAG GCGGAGGTTG CAGTGAGCAG 1920 AGACTGCACC ACTGCACTCC AGCCTGGGCA GTAGGGCAAG ACTCTTTCTC AAAAAAAAAA 1980 AAAAAAAAAA GACTCAGCAA GCAACCTTAT TCCCCCTTCT TCTGCCTGCT TTGTTCTAGC 2040 TGCACTGGCA GCTGGTTGGA TGGTGTCCAC CCATACTGAG GGTGGGTCTT TCTCTCCCAG 2100 TCCACTGACT CAAATGTCAG TCTCCTTTGA CAACACCAAC ACATACACAT CCAGGAACAA 2160 TACTTTACCA GGCATCTAGA CATCCCTCAA TCCAGTCAAG TTGACACCTA ATATTAACCA 2220 TTACATGTAT CAGGCAAATA TCTTTGTCTT CCTCTTATTC CCTTATGTAA CATAAGACAC 2280 GGTGGCTCAC ACCTGTAATC CCAGCACTCT GGAGGCCAAG GTGGGAGGAT TGCTTGAGGT 2340 AAGAAGTATA TATATATATA ATATATATAT TATATAATAT ATTATATTAT ATATAATATA 2400 TTATATAATA TATATAATAT ATTATATTTA TAATATATTA TATAATATAT AATATATTAT 2460 ATTTATAATA TATTATATAA TATATAATTA TATATATTAT ATATTATATA ATATATATAA 2520 TAATTATATA ATTATAATAT ATATTATATA ATATATAATA TATAATTATA ATATATATAT 2580 TATATATATA ATATAATATA TATAATATAA TATATAATAT ATATATATAT AGAGAGAGAG 2640 AGAGACAGAG AGAGAGAGAG ACAGAGAAAT TGCATTTGTG CTTTTTCGGT AATATTTAAG 2700
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