Variant report
| Variant | rs17093452 |
|---|---|
| Chromosome Location | chr14:63333940-63333941 |
| 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:11)
| rs_ID | r2[population] |
|---|---|
| rs11158450 | 1.00[CEU][hapmap] |
| rs12147053 | 1.00[CEU][hapmap] |
| rs12147370 | 1.00[CEU][hapmap] |
| rs12147372 | 1.00[CEU][hapmap] |
| rs12184955 | 1.00[CEU][hapmap] |
| rs12372901 | 1.00[CEU][hapmap] |
| rs17764609 | 1.00[CEU][hapmap] |
| rs2002267 | 1.00[CEU][hapmap] |
| rs7158012 | 1.00[CEU][hapmap] |
| rs7158179 | 1.00[CEU][hapmap] |
| rs7161020 | 1.00[CEU][hapmap] |
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 | nsv902015 | chr14:63261862-63356253 | Enhancers Weak transcription ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 2 | nsv1042953 | chr14:63314591-63384260 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
