Variant report
| Variant | rs9592635 |
|---|---|
| Chromosome Location | chr13:69983244-69983245 |
| allele | A/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:14)
| rs_ID | r2[population] |
|---|---|
| rs17663302 | 1.00[CHB][hapmap] |
| rs17785609 | 1.00[ASN][1000 genomes] |
| rs2325188 | 1.00[CHB][hapmap] |
| rs2325189 | 1.00[CHB][hapmap] |
| rs9317808 | 1.00[CHB][hapmap] |
| rs9317809 | 1.00[CHB][hapmap] |
| rs9541891 | 1.00[CHB][hapmap] |
| rs9541892 | 1.00[CHB][hapmap] |
| rs9541893 | 1.00[CHB][hapmap] |
| rs9541894 | 1.00[CHB][hapmap] |
| rs9541895 | 1.00[CHB][hapmap] |
| rs9541896 | 1.00[CHB][hapmap] |
| rs9599450 | 1.00[CHB][hapmap] |
| rs9599451 | 1.00[CHB][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 | nsv900479 | chr13:69824819-69984297 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
| 2 | nsv900480 | chr13:69891861-70027794 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
