Variant report
| Variant | rs34054060 |
|---|---|
| Chromosome Location | chr2:21387695-21387696 |
| allele | A/G |
| 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 |
rSNPs within LD-proxies of this variant (count:29)
| rs_ID | r2[population] |
|---|---|
| rs11124434 | 0.91[EUR][1000 genomes] |
| rs11682662 | 0.97[EUR][1000 genomes] |
| rs11683495 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
| rs11688672 | 0.94[EUR][1000 genomes] |
| rs11690364 | 0.80[EUR][1000 genomes] |
| rs12470574 | 0.91[EUR][1000 genomes] |
| rs12477767 | 0.94[EUR][1000 genomes] |
| rs12618519 | 0.94[EUR][1000 genomes] |
| rs12619256 | 0.84[EUR][1000 genomes] |
| rs12997825 | 0.95[EUR][1000 genomes] |
| rs13003754 | 0.91[EUR][1000 genomes] |
| rs13010526 | 0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs13019377 | 0.88[EUR][1000 genomes] |
| rs13022408 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs1400713 | 0.95[EUR][1000 genomes] |
| rs1914457 | 0.80[EUR][1000 genomes] |
| rs2030195 | 0.94[EUR][1000 genomes] |
| rs2048933 | 0.83[EUR][1000 genomes] |
| rs2048934 | 0.83[EUR][1000 genomes] |
| rs34144010 | 0.97[EUR][1000 genomes] |
| rs34464539 | 0.87[EUR][1000 genomes] |
| rs35112647 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs35168234 | 0.87[EUR][1000 genomes] |
| rs35750610 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
| rs4387830 | 0.82[EUR][1000 genomes] |
| rs4574146 | 0.84[EUR][1000 genomes] |
| rs6749313 | 0.91[EUR][1000 genomes] |
| rs7557098 | 0.94[EUR][1000 genomes] |
| rs7567650 | 0.94[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv873728 | chr2:21250914-21460786 | Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:21383200-21388200 | Weak transcription | HepG2 | liver |
