Tag | Content |
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EnhancerAtlas ID | HS116-15832 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr18:9173580-9175360 |
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) |
KLF4 | MA0039.3 | chr18:9174642-9174653 | CCACACCCTGC | + | 6.62 | NFE2L1 | MA0089.2 | chr18:9173840-9173855 | AAGGCTGAGTCATTC | - | 6.14 | POU2F2 | MA0507.1 | chr18:9175286-9175299 | ATATGCAAATTCT | - | 6 | RREB1 | MA0073.1 | chr18:9173603-9173623 | GGTGGGGTGGTGGGGGGGGG | - | 7.36 | ZNF740 | MA0753.2 | chr18:9173614-9173627 | GGGGGGGGGGTAG | - | 6.13 | ZNF740 | MA0753.2 | chr18:9173612-9173625 | GTGGGGGGGGGGT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr18 | 9173582 | 9173632 | chr18 | 9173878 | 9174287 | chr18 | 9174761 | 9175238 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I009173 | chr18 | 9173902 | 9174798 |
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Enhancer Sequence | CCTTCCCTTG GGAGCTCCAT CCCGGTGGGG TGGTGGGGGG GGGGTAGGGG GGGCAGTACT 60 GACCTGTTGC CAGCCTGGAT GCTGCTGTAG AAGGTGTCTG GAGATCCCCG TTAGGAGGTC 120 TCACCCAATC AGGAGGGACA GGATCAGGGA CCTGCTTAAA GATGCAGTCT GGTTGCTTTT 180 TGGTAGATCA GGTGTGCTGA ATTGGGGGTA ACCGTTCCTT GCCCAGACTG CCTGGACTCT 240 CCAGAGCCAG CCCGCTTAGA AAGGCTGAGT CATTCGTGTA CCCTAAAACT TAAAGTATAA 300 AAAAATAATA AGAAGAAGAA AGGCTTAGTC AACTGAACCG CAGAGACATT GGGCACTCCT 360 CCCCCTAGGG GCTTGTCCCA GGGAGAGATC AGAGTACTGT TCATATAACC TTGGCTGGAG 420 TTGCTGAAAT TCCCTCAGGG AGGCCCCACC CAGTGAGGAG GGATGGATTG GGGTCCCACT 480 TAAAAGAGCA GTCTGGCCAC GATCTGGCAC AGCAGCTGTG CTGCCCTGTG AGGGACTCCT 540 CCTCATCAGG ACCACCTGGA TTCTTGGGAG CAGGCTAGAA CAGCTGGGTC AACTGAACTG 600 CAGAAATGGC AGCCGCCCCT CCCCCTGAAA ACTCATCCAT TTTAGGCAGT CTCTAGCCTG 660 TTGCACTGGC TGGCTAGAAT TCAAAGCCAG TGGGTTGAGG TGCCATGGAA GTGAGGCCCG 720 CAGAATGACA CTGCTTGGTT CCCAGGATTC AGCCCTCTTC CTAGGGGAGG ATACGGATGG 780 ATTTCTCACC TTGTTGGGAT TCCCAAGGGT GGAGTCTGTA AAACTCCTGG GTTTACGTGT 840 GAGCCTGAGC AACTGCTCTG CCAAGACTCC GCACAGCTCT GTATGTTGGA CCTAAGTAAG 900 GCCCTGGTGG CCTGGGTTCA TGAGGGGATC TCCTGATCCA TGGTTGCAAA GATCCGTAGG 960 AGAAGTGTGG TTTCCTGAGT GGGGTTACAC AATCACTCAC TGCTTCCCTT GGCTGGGGGT 1020 GGGGGTTCCT TTGGCTCCCC AGTGCTCCTG GGTGGGCCAT TGCCACACCC TGCTTTTTTT 1080 GTTGTCTGTG GGTCATGCCA TCCTCCTAAT CAGTCCCAGT GTGAGAACCT GGACATTTCA 1140 TTTGAAGGTG CTGAATTCAC TTGCTGTTGT CATTCTTCTC TATGAGAGCC ATCTTGTTTC 1200 TAATCGGCTA TCTTGGCCCC TCCTGCCCCC TTCTTGTCTT ACAGGTGGAA ACTGAGGAAT 1260 AATCCCAGTG CTTTGTGAAA CTGCTATGAA GAATATTCAA GTCAGACTTA AGTTGGAAGA 1320 TAGTGACTAG AGCAAACAGA CCAAAGCATT TATTTATTTA TTTATTTATT TATTTAATTT 1380 GTTCATTCCT GAGACAGAGT CTTGCTTTGT TGCCCGGGCT GGAGTGCAGT GGTGTGATCT 1440 CGACTCACTG CAACCTCCAC CACCCAGATT CAAGCAACTC TCCTGCCTAA GCCTCCAGAG 1500 TAGCTGGGAA TACAGGCGTG CGTCACCACT CCTGCCTAAT TTTTTGTATG ACCAAAGCAT 1560 TTAAAGCATT GATTCTGAGG GCCTGGAACT CACTAAATGC TGCCAGACTC TAAAGTGATC 1620 TCAAAATAGA CTTTCTGTAG TTGGAATACT TCTGTAGATA TTCACTTGTA TTATACATGT 1680 GCAGTCTCCA TGTTTGTAGC ATTCAGATAT GCAAATTCTA TTATTTCTGT TCCCCATAGT 1740 CCTCTAGGCC ACATTGGCAA CTAGAGGTGT TTTTTTCTCT 1780
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