Variant report
Variant | rs1353679 |
---|---|
Chromosome Location | chr3:180284461-180284462 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1532485 | 1.00[CEU][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap];0.93[EUR][1000 genomes] |
rs1603658 | 0.95[EUR][1000 genomes] |
rs17707963 | 0.83[EUR][1000 genomes] |
rs17708913 | 0.91[EUR][1000 genomes] |
rs17764356 | 1.00[CEU][hapmap] |
rs28385473 | 0.91[EUR][1000 genomes] |
rs28495789 | 0.91[EUR][1000 genomes] |
rs62291004 | 0.88[EUR][1000 genomes] |
rs62291005 | 0.90[EUR][1000 genomes] |
rs62291006 | 0.91[EUR][1000 genomes] |
rs62291007 | 0.91[EUR][1000 genomes] |
rs62291008 | 0.90[EUR][1000 genomes] |
rs62291009 | 0.90[EUR][1000 genomes] |
rs62291043 | 0.95[EUR][1000 genomes] |
rs62291045 | 0.93[EUR][1000 genomes] |
rs62291048 | 0.93[EUR][1000 genomes] |
rs6443700 | 0.88[YRI][hapmap] |
rs6770664 | 1.00[CEU][hapmap];0.95[EUR][1000 genomes] |
rs6774942 | 0.95[EUR][1000 genomes] |
rs6791597 | 0.84[MEX][hapmap];0.88[YRI][hapmap] |
rs7645817 | 0.87[YRI][hapmap] |
rs7647210 | 0.84[MEX][hapmap];0.88[YRI][hapmap] |
rs9290705 | 0.86[EUR][1000 genomes] |
rs9819839 | 0.84[EUR][1000 genomes] |
rs9837678 | 0.93[EUR][1000 genomes] |
rs9846858 | 0.91[EUR][1000 genomes] |
rs9847201 | 0.84[EUR][1000 genomes] |
rs9857489 | 0.91[EUR][1000 genomes] |
rs9858483 | 1.00[CEU][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap];0.91[EUR][1000 genomes] |
rs9864959 | 0.84[EUR][1000 genomes] |
rs9866580 | 0.84[EUR][1000 genomes] |
rs9872076 | 0.84[EUR][1000 genomes] |
rs9876153 | 0.95[EUR][1000 genomes] |
rs9877497 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1007831 | chr3:180162003-180348203 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv536818 | chr3:180162003-180348203 | Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:180282600-180284600 | Enhancers | Ovary | ovary |
2 | chr3:180284200-180284800 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |