Variant report
| Variant | rs11834730 |
|---|---|
| Chromosome Location | chr12:62400460-62400461 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:2 , 50 per page) page:
1
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:16)
| rs_ID | r2[population] |
|---|---|
| rs10506433 | 1.00[YRI][hapmap] |
| rs11832185 | 1.00[YRI][hapmap] |
| rs11836702 | 1.00[YRI][hapmap] |
| rs11836835 | 1.00[YRI][hapmap] |
| rs11837421 | 1.00[YRI][hapmap] |
| rs11837618 | 1.00[YRI][hapmap] |
| rs17654807 | 1.00[YRI][hapmap] |
| rs17656359 | 1.00[YRI][hapmap] |
| rs17656662 | 1.00[YRI][hapmap] |
| rs17705009 | 1.00[YRI][hapmap] |
| rs17706308 | 1.00[YRI][hapmap] |
| rs17713184 | 1.00[YRI][hapmap] |
| rs3892748 | 1.00[YRI][hapmap] |
| rs9669548 | 1.00[YRI][hapmap] |
| rs9737799 | 1.00[YRI][hapmap] |
| rs9739100 | 1.00[YRI][hapmap] |
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 | nsv1039741 | chr12:62046850-62491052 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
