Tag | Content |
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EnhancerAtlas ID | HS156-05992 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr19:4828820-4831620 |
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 | chr19:4829482-4829498 | TGGGACAAAGTCCACT | + | 6.39 | ZNF263 | MA0528.1 | chr19:4829764-4829785 | TTTTTCTCTTCCTCTTCCTTT | - | 6.08 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27604 | chr19:4829059-4829695 | Esophagus | SE_27604 | chr19:4830051-4832224 | Esophagus |
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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 | TCTCCTGCCT CACCCTCCCG AGTAGCTGGG ACTACAGGTG CATGCCACCA TGCCCAGGTA 60 ATTTTTGTAT TTTTAGTAGG GACGGGGTTT CACCATGTTG GCCAGGATGG TCTCAATCTC 120 TTGATCTCGT GATCCGCCTG CCTTGGCCTC CAAAATTCTG GGATTACAGG CGTTAGCCAC 180 CACGCCCTGC TAGTTTTTGT AATTTTAGTA GAGACAGGGT TTCAGGCTGT TGGCCAGGCT 240 GGTCTCGAAC TCCTGACCTC AATCGATCCG CCTGCCTTGG CCTCCCAGAG TGCTGGGATT 300 ACAGGCATGA GCCACTGCGC CCGGCCTGTA TAGGACTCTT AAAGCAGTGC CTGGCACACG 360 CATGCCCCAC AAACATTAGC ATGCAAGACT GAAACCTCCT TGCAAGAAGG ACTCAGGGGA 420 GTTTTGCAGA AAACACGACA AAGCCAGCCA GACTTAGAAT CATCAAGGCA GGACCATCTC 480 CACCTGAATG CCTGGCAAAT CTCTAAAATC ACGTGGTCTT TCTTCTCATT CTCTCTGCCC 540 CCCCGGGCCT GAACTCAACT CTATTTCAGT GACTGCCCCA GCTTCCCCCG CCCGCCTCCC 600 CTGCCCACTG CCACCTCCAC CTTCTCGAGA CCCAGCAAGT TTCATTTCTC ACTGTCCATG 660 GCTGGGACAA AGTCCACTCC TCACTCTGAA GAGCAGGCGC CTGGCGGGAC AAAAACACCC 720 ATGGGGTAGG AGGGTTCTGG CTCTGCCACC TGCCGGCTTG TGTGGTCTGT TTCTCAGCCT 780 CAGCTTCCTC ATTTATAACA CCCACATGAA CTGGTACTTA GGATGAATGG GAGTCTGTTT 840 TGAAGCTTTC ATGCGAAAAT ATGGTTAAAA AGTTTAGATC AGTGCCCAGC AAGGAGCAAG 900 AGCTTGATAT AATAATATTA GTGTGACAAT AAATATTGGC AGACTTTTTC TCTTCCTCTT 960 CCTTTTTAAA AAAATTTTTG ATTTTTAATT TCATTTCTTT TTTTTTTTTT TTTTTTTTTT 1020 GACACAGAGT CTTGCTGTGT CGCCCAGGCT GGAGTGCAGT GGCGTGGTCT GGGCTCACTG 1080 CAACCTCCGC CTCTTGGGTT CAAGTGATTC TCCTGCCTCA TCCTCCTGAG TGGCTGGGAT 1140 TACAGGCATG CACCACCACG CCCCGCTAAT TTTTGTATTT TTAGTAGAGA CAGGGTTTCG 1200 CCATGTTGGT CAGGCTGGTC TCAAACTCCT GACCTCAGGT GATCTGCCTG GGATTACAGG 1260 CGTGAGCCAC CTGCCCAGCC CCATTTCATT TTTTTTAGAG ACAGGGTCTC ACTCTGTCAC 1320 CCAGGCTGGA GTGCAGTAGT GGGATCACGG CTCACTGCAG CCTTGAACTC CCGGGTTCAA 1380 GTGATCCTCC CACCTCAGCC TCCCGAGTAG CTGGGACTAC AGGTGTGCGG CACCACACCT 1440 GGCTAATTTT TGTATTTTTG GTAGAGACAG AGTCTCACCC ATGTTACCCA GGATCCTGGG 1500 CTCAAGCAAT CCACCTGCCT CAGCCTCCCA AAGTGTTGGG ATTACAGGCA TAAACCACTG 1560 CACCCGGCTA ACTTTCTTTT TGAATTTTTT TGTAGAGGTG GAGTCTCGCT ATGCTGCCCA 1620 GGCTTGTCTT GAACTCCTGG GCTCAAGTGA TCCTCCCACC TTGTCCTTTT TAAATGTTTT 1680 AACCACCTCT CCCACTCTCC TTCCCACACT CTCATGCAGC CTTTCATGCA TCGAATATGC 1740 ATTTATTGAG CACCTACTAG GTCCAGGAAC TGTTCAAAGT GCCACTGCAT ATCAAGGCAG 1800 GCACATCTAC CCTCACAGAG CTCCCAGTCT GGTTCAGGGA GACCAACAGT AAGCGAGAAA 1860 ATAACCCAAG ATCATTTCAG AGAATGAAAA GTAACGTGAA AGCCATGAGC CGGGGGCTGT 1920 GTGGCTCTGA GAGACTGGCT GGGAAGGGGC TACAGGGGAC CACGGTGGTC AAGGGAGGCC 1980 TTTGGGGACA GGAGGTAACA TTGAGCTGAG ACCTAAAGGA GCTGAGGGAG GAGGCTGGGT 2040 GGAGATCAGG GAGGAAAGCT TCTGGAAGGT GAAGCCACCT GCCCAAAGGC CCTGGGGCAG 2100 GACTGCGCCT GGTGAGCTGG AGGAACAGTA AGGAAGCCCA TGTGGCTGGA TAACCGTTAG 2160 GAGGGGGAGA AAGGAAGAAG GTGTGTGGTG GTACAGGGTG TGAGGTTGGG ATCCTGGGTG 2220 TCAGGGAAGA GTTTGGGGTG TCAGGGAGGA ATTTGGGGTG TCTGGGAGGA ATCTGGGGTA 2280 TTCGGGAGGG ATCCTGGGTG TTGGGGAAGA ATCCAGGGTG TCAGAGAGGG GTCCTGGGTG 2340 TCACGGAGGA ATTTGGGGTA TCAGGGAGGG ACCTTGGGTG TCAGGGAGAA ATTCAGGGCG 2400 TTGAGAGAAA TATGGGGTGT GAGGTAGGAA GCTTGGGTGT CAGGAATTTG GGGTGAGAAG 2460 GAATATGGGG TTTCAGGTAG GAATCCTGGG TGTTGGGGAG GAATCTGGGG TGTCCGGGAG 2520 GAATCTGGGG TTTGGGGGAG GGGTCAGGCT GTCGGGGAGG AAGCCAGGGT GCTGGGGAGG 2580 ATCCCGACAG TGGGGGAGGA TCTGGGCCAC CAGCGCGGGG AGCTGGAGGT TGAGGGGAAC 2640 GTCAACCTCC CAACGCGCGG CGCCAGGCCC CCTCCTCCGC ACCGGGGCCC TAAGAGGGAG 2700 GCCAGGTGGC CTGGAGCCCT GGCGAGCGGC ACGGGCTCAG GGCCACCCCC CACACCCCCG 2760 ACACCTTCTC CACCTCAGGC CCGTCCTCGC CCCTTCCCCA 2800
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