Variant report
| Variant | rs11710987 |
|---|---|
| Chromosome Location | chr3:102104625-102104626 |
| allele | A/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 |
rSNPs within LD-proxies of this variant (count:11)
| rs_ID | r2[population] |
|---|---|
| rs11708036 | 1.00[ASN][1000 genomes] |
| rs11716985 | 1.00[MEX][hapmap] |
| rs1585775 | 1.00[ASN][1000 genomes] |
| rs4566515 | 1.00[ASN][1000 genomes] |
| rs58002972 | 1.00[ASN][1000 genomes] |
| rs72947064 | 1.00[ASN][1000 genomes] |
| rs72947069 | 1.00[ASN][1000 genomes] |
| rs72947082 | 1.00[ASN][1000 genomes] |
| rs72949082 | 1.00[ASN][1000 genomes] |
| rs72949091 | 1.00[ASN][1000 genomes] |
| rs7637411 | 1.00[ASN][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 | nsv877227 | chr3:102067254-102184308 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
