Tag | Content |
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EnhancerAtlas ID | HS091-22788 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:2241350-2243380 |
Target genes | Number: 20 | 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) |
Hnf4a | MA0114.3 | chr19:2242290-2242306 | GGGGTCAGAGTCCAAA | + | 6.81 | REST | MA0138.2 | chr19:2241647-2241668 | GCAGTTCTCCCTGGTCCTGAA | - | 6.94 | SOX10 | MA0442.2 | chr19:2241781-2241792 | TTCTTTGTTTT | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr19 | 2242184 | 2242549 | chr19 | 2242790 | 2242840 | chr19 | 2242908 | 2243073 | chr19 | 2242200 | 2242600 |
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Enhancer Sequence | GGTTTCTGTG ATGTGTGGAG AGGCAAGTGC GGCTGCGGCC TGGTGGGAGG CTGCTTGCTG 60 GGCTCCCCAC GCACGTCCCC TGATGTGAGT TTCATGTCAC TTGACCAGGA AATGCTTGAA 120 TGTCCTCCAG AGAAAAATGA GGCACTTCAT GAACCTGTCC GGGCGGCACC CACACAATCC 180 TGCCCGCCTG TGGGCCGTCC GGAGACAGAA CCTCCCAGGC AGCTGTAAGC TGTTGTGGCA 240 GCAGGGACTG TAGGAGTTGG CGTGGCCTGC AGCTGACGGC GCCAGCATGG AGAGGGTGCA 300 GTTCTCCCTG GTCCTGAAGA ATGTGTGGCC AAGAAGCCCG AGGCGGGGAG GGTTCCTTGG 360 GGCCAGAGGG TGGCGTTCCC AGCAAAGGAC AGTCCTTCTG GTGTCACAGT CTCCTTTTTC 420 ACACTGGAAT GTTCTTTGTT TTGTGAAGGG ATGGCGATGG TCACAGTGGT GGTTTCTCGA 480 AGTTTACGTG ACAACATGTA AAAATGGGCA TCTCTAGGTG GGCTTTTGTG ACATCTGAAC 540 TTCTGATGGG GCAGCCGTGA TACTGCAGTG AGCTGGGAGG TCCACCTCAC CAGTTACCAT 600 GCTTGATCAT TTTCATAAAC TTGCCCAGGG AATAAAAACT GGTTGGGGAG GGCTCCTGGG 660 CCCCCATAGA GTAAGGGGTG ACTTCAGGCC CCACCACAAG TCAGCAGTAC AGCTGGCCTG 720 TCCCTCAGCA TGCCCCTGCA CACCTGCGGC CACTGTGGCC TGTCCCTCAG CGTGCCCCTG 780 CACACCTGCC GCCACTGTGG CCTGTCCCTC AGCGTGCCCC TGCACACCTG CGGCCACTGT 840 GCCCTGTCCC TCAGCGTGCC CCTGCACACC TGCAGACACT GTGACACATC ACTGCAGACG 900 CAGTAGTTCA GATGACACGG CTGTATCAGC TTCTGGTTCT GGGGTCAGAG TCCAAACAGT 960 CCACAGGGCT CCATTCCTTC TGGAGGCTCT GGGGGACAAC TCGTTTCCTG CCTTTCCCAG 1020 TGTCCAGAGG CACCTGTGTG CCTTGCCTCG GGGCCCCTTC CTCCCCATTC ACAGCCACAG 1080 CGCAGCCTCT CTGACTCTCA GCCTCCCGCC TCCTCTCATG AGGTCACCCA GGATCACCTG 1140 CCATTTTAAG ATCCTCAAGC CCACCTGCAC ATCCCTTTTC TGCCATGAGG GGACATGTTC 1200 ACAGGTCCCA GGGATTAGGA TGTGGACATC TTTTGGGGGC AGTGATTCAC TCAGTCTCAT 1260 GGGCCCCATC TCTCTGAGCT CACCCAAGAC CCTTAAACCA GGGCCCGGGG CCAACATTGA 1320 GCAGGCAAGG GAAAGACTAC CAGGAGATGA GAGGAGGCTG CCTGGAACTC AGATTTGCAC 1380 AGAGCCTGAA AGGGCGTGGG AGACCTTGGC AGAGGCCTGC ATCAGGAAGA GGATGTTGGG 1440 GACTCAGCAG AGCCCCCTGC GCCACAAGCA GATGTGGCAG ATCTCCCAGG TGTTACTCAG 1500 TGAGGATGCG AAGATCAGTG TCCTCACTGA TCTCCGCCTA ACAAATTTAC ATCGAGCCCA 1560 AGAGATTAGG TTGGGACAAG TAAGCGTAGC CAACCAGAGA GGGAATTCAG AGGAAGGCGT 1620 GAACACTAGG GGCTTGGGCA GTCCGGGATG GCTTCCTGGA GGTGGTGACT CGTTTGTGAG 1680 ATCTTGGTCT TGTCTTCCCT TTATGCCTTC TCTGGGCTCC CTATTACAAT TTCAGGTCTC 1740 CAGGCCTTGG CACCCTGGGC TGGAGCGGCT TCCTCTCCAT CCCTCATGCC TGGTCACTTG 1800 GAGACAGGCT CCAGCTTCCT TGTGTCTGTG CCTGTCCACA GTGGGCCTCA GCCTCCTGGA 1860 AGAGACTGGG TGCGCTATGG GGTGGCCCCC TCAGGGCTGG TTAGACCCTG GCGCTGGGAG 1920 TGCAGGGTGA GGGGCAGTCT CGAGGGCTCC AGCCCAGCCC GCCCAGGGAG GTCCCAGCAG 1980 CAGCCCCGAG TTCTGAGCCA TCTTCCTCAC TCTCCTCTTG GCCTCCACAG 2030
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