Variant report
| Variant | rs35651857 |
|---|---|
| Chromosome Location | chr14:63198572-63198573 |
| allele | C/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:10)
| rs_ID | r2[population] |
|---|---|
| rs1032306 | 1.00[CEU][hapmap] |
| rs11158447 | 1.00[CEU][hapmap] |
| rs17100325 | 0.88[MEX][hapmap] |
| rs2355061 | 1.00[CEU][hapmap] |
| rs2355062 | 0.81[JPT][hapmap] |
| rs7141868 | 1.00[CEU][hapmap] |
| rs7147349 | 0.88[MEX][hapmap] |
| rs8020611 | 0.88[MEX][hapmap] |
| rs8022441 | 0.88[MEX][hapmap] |
| rs915064 | 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 | nsv527675 | chr14:63168547-63211280 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 2 | nsv976814 | chr14:63192257-63202004 | Enhancers ZNF genes & repeats Weak transcription | n/a | n/a | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
