Variant report
| Variant | rs1849541 |
|---|---|
| Chromosome Location | chr4:21837689-21837690 |
| allele | C/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:27)
| rs_ID | r2[population] |
|---|---|
| rs10002735 | 0.83[AMR][1000 genomes] |
| rs10021306 | 0.83[AMR][1000 genomes] |
| rs10025080 | 0.83[AMR][1000 genomes] |
| rs10033262 | 0.83[AMR][1000 genomes] |
| rs11934767 | 0.83[AMR][1000 genomes] |
| rs11939350 | 0.83[AMR][1000 genomes] |
| rs11943657 | 0.83[AMR][1000 genomes] |
| rs1913333 | 0.93[YRI][hapmap] |
| rs28379252 | 0.83[AMR][1000 genomes] |
| rs28452597 | 0.83[AMR][1000 genomes] |
| rs28475189 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs28547323 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs28578495 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes] |
| rs28676618 | 0.83[AMR][1000 genomes] |
| rs28754425 | 0.83[AMR][1000 genomes] |
| rs55842595 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs6827460 | 0.83[AMR][1000 genomes] |
| rs6833077 | 0.83[AMR][1000 genomes] |
| rs73105917 | 0.83[AMR][1000 genomes] |
| rs73108038 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs7664829 | 0.83[AMR][1000 genomes] |
| rs7681022 | 0.83[AMR][1000 genomes] |
| rs7695914 | 0.83[AMR][1000 genomes] |
| rs7699892 | 0.96[YRI][hapmap] |
| rs986698 | 0.80[YRI][hapmap];0.83[AMR][1000 genomes] |
| rs9991759 | 0.83[AMR][1000 genomes] |
| rs9999185 | 0.83[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv817467 | chr4:21602921-22422816 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
| 2 | nsv291226 | chr4:21833309-21839155 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr4:21837000-21837800 | Enhancers | Muscle Satellite Cultured Cells | -- |
| 2 | chr4:21837200-21837800 | Enhancers | HUVEC | blood vessel |
