Tag | Content |
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EnhancerAtlas ID | HS091-23912 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:36150140-36152410 |
Target genes | Number: 28 | Name | Ensembl ID |
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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) |
Foxo1 | MA0480.1 | chr19:36151805-36151816 | TGTAAACAGGA | - | 6.62 | Nr2f6(var.2) | MA0728.1 | chr19:36150552-36150567 | 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 | TGTGCCAGTC AATGAGTCAA ATAGTTGATT ATACAGAATA ACCTAAGTTC CTATGTGTGC 60 AACCACCCTA CATAATTTTA AAGCAAATTA TATAGATTAT AATATAATAT AAAATACATA 120 AAGATTATAT TTTATCCAGA AATAAGAAAC TATATGTATC TCTTGGAGAT ACAATTTTTT 180 TTTTTTTTTT TTTGAGACAG AGTCTCAATC TGTTGCCCAG GCTGGAGTGC AGTGGTGTCA 240 TCTCAGCTCT CTGCAACCTC TGCCTTCTGG GTTCAAACTA TTCTCCTGCC TGGAGATACC 300 TATTTTTTTA ACATAATTAT TTACACCTAA GAAATTAGTT CTTAATGGCC GGGCACAGTG 360 GCTCATGCCT GTAATCCCAG CACTCTGGGA GGCTGAGGTG GGCAGATCAC CTGAGGTCAG 420 GAGTTCAAGA TCAGCCTGGG CAACATGGCG AAACCTCGTC CCTACTAAAA GTACAGAATT 480 AGCCAGGCAT GGTAGCACAT GCCTGTAATC CCAGCTACTC GGGAGTCTGA GGCAGGAGAA 540 TCGCGTGAAC CTGGGAGGCA GAGGATGTGG TGAGCCGAGA TCATGCCATT GCACTCCAGC 600 CTGGGCAACA AGAGTAAATC TCCATCTCAC CAAAAAAAAA AAAAAAAAAA AAAAAGAGTT 660 CTTAATATCT AATAAGCAAT CTCCTGCACA ATGTGTAACT TCTCCCCGTG TTGGGACCTG 720 CTCTTTCATG CTGATCATGA TGGTAGTTGG AAGTCATTTA AGTAGGCCAA GTTGAGAGCT 780 GTTCTTCATG GTGCCCCCAA AAGAATTGCC ACACAATAAC AGCCCAGAAT ATCCCCAACA 840 GACTCGTCAA CAGGGACCTA GCTAGCATGA CCAGCCGGAA CACTCTTATG GCTGAATTGG 900 TGTGTCCTCA AAACCTTTCA AATGGCCGGG GTGTGGTGGC TCACACCTGT AACCCTAGCA 960 CTTTGGGAGG CCCAGGCGAG TGGGTCACGA GGTCAGGGAT TCAAGACCAG CCTGGCCAAG 1020 CTGGTAAAAC CCCATCTCTT CTAAAAATAC AAAAAAAACT ATAAAAATAC AAAAATTAGC 1080 CAGGTGTGGT GGTGCGTGCC CCTAATCCCA GCTACTGGGG AGGCTGAGGC AGGAGAATCA 1140 CTTGAACCTG GGAGGTGGAG GTTGCAGTGA GCTGAGATCA CACCACTGTA CTCCAGCCTG 1200 GGCGACAGAG CGAGACTCCA TCCCCAAAAA ACAAAAACAA AACTTCAAAT GGTTACAAAC 1260 TTGTCTGATG CATTCACATG AGCAGGGATG ATTCTTGTAT GGAGAAAAAT GGCCCCAGAG 1320 ATAGATCTTG TGAAATAGCT GCTCATGAAG AAAAGTGGCT GTAGGGGCCG GGCGCGGTGG 1380 CTCACGCCTG TAATGCCAGC ACTTTGGGAG ACCGAGGCAG GCAGATAACC TGAGGTCGGG 1440 AGTTCCAGAC CAGCCTGACC AACATGGAGA AACCCCGTCT CTACTAAAAA TACAAAATGA 1500 GCCAGGCGTG GTGGTGCATG CCTGTAATCC CAGCTACTCT GGATGCTGAG GCAGGAGAAT 1560 TGCTTGAACC CAGGAGGTGG AGGTTGCTGT GACCCGAGAT TGTGCCATTG TACTCCAGCC 1620 TAGGCAACAA GAGCGAAACT CCGTCTCAAA AAAAAAAAAA GTGGCTGTAA ACAGGACCTT 1680 AGTGCACACA CAGGGAGCTT GAGGGATCGT GGGAGGTTAT GGCGTGGGTT GGAAGTAGCA 1740 AAGAACTTAA ACACCATGAA AAAAAAATTT TTTTTTTGAA ATGGAGTCTT GCTCTGTTGT 1800 CCAGACTGGA GTGCAGTGAT GTGATCTCTG CTCACTGCAA CCTCCACCTC CCGGTTCAAG 1860 CAATTCTGCC TCAGCCTTCC AAAACGCTGG GATTACAGGC GCTTGCCACC ACACCCAGCT 1920 AATTTTTTGT ATTTTTAGTA GCGATTTAGA GAGTAGTTTC ACCGTGTTGA CCAGGCTGGT 1980 CTTGAACTCC GTGACCTCAG GTTAACCATC CACCTCGGCC TCCCAAAGTG CTGGGATTAC 2040 AGGCATGAGC CACCACACCC AGCCAACACC ATGAAAATTT CAAATGAAAC AGGACGGCCA 2100 GTGAAAAGTC AAGGTGCTGG ACTCCTTGAG TCCAGCTGCC TGATTCTGCC CAGGGTTTGC 2160 CACCAGTGCC AGTGTTTCCT GTACATTCCT TTAGAGATAG CTCATGCATC TAGAAGTATT 2220 TGTAAATATA TTGATCTGAT TGGATATGGT GCCCTTTTGC TCACACAGCC 2270
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