Tag | Content |
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EnhancerAtlas ID | HS116-13461 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr16:31129340-31131500 |
Target genes | |
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) |
Esrra | MA0592.2 | chr16:31129399-31129410 | TTGACCTTGAA | - | 6.14 | Foxd3 | MA0041.1 | chr16:31130477-31130489 | GTTTGTTTGTTT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr16:31130689-31130704 | TGACCTCTTAACCTC | - | 7.77 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09570 | chr16:31122347-31132628 | CD14 | SE_26229 | chr16:31128868-31132413 | Duodenum_Smooth_Muscle | SE_26836 | chr16:31128082-31131019 | 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 | CTTGAGGAAA GAACGCCGCG TTCCGGGCGC TGAGAAACCA GCCGGGTTGT GGGAGGCTGT 60 TGACCTTGAA TTATGCCGAG CGACGCCTAC AAACCCACCG CTCAGGCCTT CACCAGGATT 120 GTTCCCATTC CACTTCCTTG CCCAGTCTTA GGCTTCATTC CTTTTTCTTG CTAACGCTGC 180 TTCCTCACCC TCTCTTGTCT CTGCGTCTTC TTTTTCCATT TGTCCCTGGC AGCCATCCGC 240 AGAGAGAAGA CCTTCCAGAA ACAACAGGCT TCCCTTTCCT AAAGTTCTGC TGCCTTCTCT 300 CATTTTCAAA ATTAACCCCA AACTCCTTAG GGTGGCATTC ATTTTTGTGA CCTCTCCAGT 360 TTCTAGCCAA CACTAGGAAA GGGCATTGCC AGGCCAGAAC ACACTGTGCC CTCTGAAGAC 420 CACACGCCCT TTACCACCTG TGCCCTTTGC TTGGAATGCT TTTTCTTCCC TTTCTCCTTG 480 TTTGCCTGCC TAGCTCCTAC TCATCCTCTT AGCTTCATAT CCTTTGTGAT GTCATCCTTG 540 ATTCCCCTTC AGGCAAAGTG AGTGGTTCCC TTCTCTATGT TCCTGCAACA TTTTTTTCCT 600 ACCTCAGTCA TAGTTTTTGT AACATTATGT TGTAATTTTC TCTCTCTGTC TTCCTCCATC 660 ATACTGGGAA CTTCTGGAGG GCAGCACTTC TTGTGATTCA TCACTGTGTC CTCTGTACCC 720 GGCAACAACA CAGCATAGGG CCAGACACGT AGTGGTTGCC TTACTCATTT ATTGAATGCT 780 CTGCTAATTG TCAGGTGCGC TGCTAAAAAT TTTGGAGGCA TTAATTCACC TTCTAAGGTT 840 GGTACTATTA TCCCTTTTGT CTTTTTTTTT TTTTTTTTTT TTGAGACAGG ATCTCGCTCT 900 GTCACCCAGG TGGGATTGCC GTGGCACGAT GACAGCTCAC TGAAGCCTAG ACCTTCTAGG 960 CTCAAGTGAT CCTCCCACCT CACCCTCTCA GAGTGTTGGG ATTACTGGCA TGAGCCACTG 1020 TGCCCAGCTG TTATCCCTTT TCACAGATGA AGAGACTGAG GCTCAGAAAG ATGGAATAAC 1080 TTGCTCAGTT ACACATAGCT AGGAAGTAGG GAGCTGGAAT TTTGTGTATT TTTTTTTGTT 1140 TGTTTGTTTG AGATGGAATC GCTCTCTGTT GCCAGGCTGG AGTGCAGTGG CGCCATCTTG 1200 GCTCACTGCG ATCTCTGCCT CCCGGATTCA AGCGATTCTC CTGCCTCAAC CTCCTGAGTA 1260 GCTGGGACTA CAGTTGTGCG CCACCACACC CAGCTAATTT TTGTATTTTT AGTAGAGACG 1320 AAGTTTCACC ATGTTGGCCA GGATGGTTTT GACCTCTTAA CCTCGTGATT CACCCACCTC 1380 GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACGAT GCCCAGCCCT GGAATTATAC 1440 ATTAATGTAG GTTATCTTAA TCCAGAGCCA GCACTCATGA TCCCTGAACA AATGAACAAC 1500 TGCGGGTATG TGGTAAAATG AGCATTGAAT TTAGAGTCAG ACTTAAATTC AGTTAAGTAT 1560 TAGCTCTTAC CACTTTTCAA ATCTGTGACC CTAGGTAAGC CTCAGTTTTG TTCTGTTTTT 1620 TGGGGTTCTT TTTTTTGAGA CAGAGTCTTG CTCTTGTCAC CCAGGCCACA GTGCAGTGGT 1680 ACAATCTCGG CTCACTGCAA CCTCTGCCTC CCGGGTTCAA GCAATTCTCC TGCCTCAGCC 1740 TTGCCTCCCA GGTTCAAGCA ATTTTCCTGC CTCAGCCTCC CGAGTAGTTG GGATTACAGG 1800 TGTGTGCCAC CATGCCTGGC TTTTTTTTTT TTCGTCTTTT TGGTACAGAT GGGGTTTTGC 1860 CATGTTGACC AGGCTGGTCT CAAACTCCTG GCCTCAAGTG ATCTGCCCAT CTCGGCCTCC 1920 AGAAGTACTG GGATTACAGG TGTGAGCCAC ACACCCAGCC AGTTATTTTC TCATTCGTAA 1980 AATGAGAATA ACAGCCTCAA CCTGATCCAC CTCACAGTTG TGGCAGTGAT TGAGTAGAAT 2040 GGCAGAGGTG GACCAGTGAG GTTAGCTGAT GTGTGGCCCT GAACTCTGGA AACTGCTTCT 2100 CAGTGTGCAG GATTCCTTTT GTTCCAGCCT TACCTTCCTG ATGACCCTAG CCTTTTTCCA 2160
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