Variant report
| Variant | rs4826922 |
|---|---|
| Chromosome Location | chrX:104648583-104648584 |
| 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:13)
| rs_ID | r2[population] |
|---|---|
| rs1156923 | 1.00[YRI][hapmap] |
| rs1292802 | 1.00[YRI][hapmap] |
| rs1321384 | 1.00[YRI][hapmap] |
| rs210726 | 1.00[YRI][hapmap] |
| rs210729 | 1.00[YRI][hapmap] |
| rs210730 | 1.00[YRI][hapmap] |
| rs210731 | 1.00[YRI][hapmap] |
| rs5916908 | 1.00[YRI][hapmap] |
| rs5916911 | 1.00[YRI][hapmap] |
| rs5916928 | 1.00[YRI][hapmap] |
| rs5916929 | 1.00[YRI][hapmap] |
| rs986468 | 1.00[YRI][hapmap] |
| rs991444 | 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 | nsv432352 | chrX:104346855-104831855 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
