Tag | Content |
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EnhancerAtlas ID | HS182-10270 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr18:9173260-9175580 |
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: 4 | Chromosome | Start | End |
chr18 | 9173582 | 9173632 | chr18 | 9173878 | 9174287 | chr18 | 9174761 | 9175238 | chr18 | 9175442 | 9175488 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I009173 | chr18 | 9173902 | 9174798 |
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Enhancer Sequence | CTTCACAATG TTGGCCAGGC TGGTCTCAAA CTTCTGATCT CAGGTGATCC GCCCTCCTCG 60 GCCTCCCAAA GTCTGAGATT ACAGGCATGA GCCACCACGC CTGGCCAGTT GCTGACCTTT 120 AAATGGGGTT TTTGTGGTGT CTTTTTTGTT GATACTCTTG TTGTTGTTTT CTGTTTTTCT 180 TTTAACAGTC AGTGCACTTT TCCATAGGGC TGCTGTAGTT TGCTGGGGGA TTGCTGCAGA 240 CCCTAGTTGT CTTGGTCTTT CCTTTACCTG TAGGTATATC ACCAGTGAAG GCTGTGAAAC 300 AGCTAAGATG GCAGTCTGCT CCTTCCCTTG GGAGCTCCAT CCCGGTGGGG TGGTGGGGGG 360 GGGGTAGGGG GGGCAGTACT GACCTGTTGC CAGCCTGGAT GCTGCTGTAG AAGGTGTCTG 420 GAGATCCCCG TTAGGAGGTC TCACCCAATC AGGAGGGACA GGATCAGGGA CCTGCTTAAA 480 GATGCAGTCT GGTTGCTTTT TGGTAGATCA GGTGTGCTGA ATTGGGGGTA ACCGTTCCTT 540 GCCCAGACTG CCTGGACTCT CCAGAGCCAG CCCGCTTAGA AAGGCTGAGT CATTCGTGTA 600 CCCTAAAACT TAAAGTATAA AAAAATAATA AGAAGAAGAA AGGCTTAGTC AACTGAACCG 660 CAGAGACATT GGGCACTCCT CCCCCTAGGG GCTTGTCCCA GGGAGAGATC AGAGTACTGT 720 TCATATAACC TTGGCTGGAG TTGCTGAAAT TCCCTCAGGG AGGCCCCACC CAGTGAGGAG 780 GGATGGATTG GGGTCCCACT TAAAAGAGCA GTCTGGCCAC GATCTGGCAC AGCAGCTGTG 840 CTGCCCTGTG AGGGACTCCT CCTCATCAGG ACCACCTGGA TTCTTGGGAG CAGGCTAGAA 900 CAGCTGGGTC AACTGAACTG CAGAAATGGC AGCCGCCCCT CCCCCTGAAA ACTCATCCAT 960 TTTAGGCAGT CTCTAGCCTG TTGCACTGGC TGGCTAGAAT TCAAAGCCAG TGGGTTGAGG 1020 TGCCATGGAA GTGAGGCCCG CAGAATGACA CTGCTTGGTT CCCAGGATTC AGCCCTCTTC 1080 CTAGGGGAGG ATACGGATGG ATTTCTCACC TTGTTGGGAT TCCCAAGGGT GGAGTCTGTA 1140 AAACTCCTGG GTTTACGTGT GAGCCTGAGC AACTGCTCTG CCAAGACTCC GCACAGCTCT 1200 GTATGTTGGA CCTAAGTAAG GCCCTGGTGG CCTGGGTTCA TGAGGGGATC TCCTGATCCA 1260 TGGTTGCAAA GATCCGTAGG AGAAGTGTGG TTTCCTGAGT GGGGTTACAC AATCACTCAC 1320 TGCTTCCCTT GGCTGGGGGT GGGGGTTCCT TTGGCTCCCC AGTGCTCCTG GGTGGGCCAT 1380 TGCCACACCC TGCTTTTTTT GTTGTCTGTG GGTCATGCCA TCCTCCTAAT CAGTCCCAGT 1440 GTGAGAACCT GGACATTTCA TTTGAAGGTG CTGAATTCAC TTGCTGTTGT CATTCTTCTC 1500 TATGAGAGCC ATCTTGTTTC TAATCGGCTA TCTTGGCCCC TCCTGCCCCC TTCTTGTCTT 1560 ACAGGTGGAA ACTGAGGAAT AATCCCAGTG CTTTGTGAAA CTGCTATGAA GAATATTCAA 1620 GTCAGACTTA AGTTGGAAGA TAGTGACTAG AGCAAACAGA CCAAAGCATT TATTTATTTA 1680 TTTATTTATT TATTTAATTT GTTCATTCCT GAGACAGAGT CTTGCTTTGT TGCCCGGGCT 1740 GGAGTGCAGT GGTGTGATCT CGACTCACTG CAACCTCCAC CACCCAGATT CAAGCAACTC 1800 TCCTGCCTAA GCCTCCAGAG TAGCTGGGAA TACAGGCGTG CGTCACCACT CCTGCCTAAT 1860 TTTTTGTATG ACCAAAGCAT TTAAAGCATT GATTCTGAGG GCCTGGAACT CACTAAATGC 1920 TGCCAGACTC TAAAGTGATC TCAAAATAGA CTTTCTGTAG TTGGAATACT TCTGTAGATA 1980 TTCACTTGTA TTATACATGT GCAGTCTCCA TGTTTGTAGC ATTCAGATAT GCAAATTCTA 2040 TTATTTCTGT TCCCCATAGT CCTCTAGGCC ACATTGGCAA CTAGAGGTGT TTTTTTCTCT 2100 CAGCCCTATC TTCTAAATAG TCTGAGTTGT CTTTCTCTGT TATTGGATTT TCTCCCTGAT 2160 TCTCCCTCCT TTTGTCAGTG TTCAGTAGTT TTTCGTCCAC AGAAATGGTC CCAAGGCTTC 2220 TTTCCTTCTT GATCACTTGA TCAGTTTTTC AAAGGCTCCT CTTTTTTTTT TTTTTTTTTT 2280 TTTTTTTTTG AGACAGTCTC TGTCATGCAG GCTGGAGTGC 2320
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