Variant report
| Variant | rs7064524 |
|---|---|
| Chromosome Location | chrX:74141191-74141192 |
| 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:15)
| rs_ID | r2[population] |
|---|---|
| rs1340989 | 1.00[YRI][hapmap] |
| rs2148096 | 1.00[YRI][hapmap] |
| rs2676492 | 1.00[YRI][hapmap] |
| rs2676493 | 1.00[YRI][hapmap] |
| rs2676496 | 1.00[YRI][hapmap] |
| rs2676498 | 1.00[YRI][hapmap] |
| rs2798171 | 0.83[YRI][hapmap] |
| rs2798172 | 1.00[YRI][hapmap] |
| rs2798173 | 1.00[YRI][hapmap] |
| rs2798174 | 1.00[YRI][hapmap] |
| rs2798175 | 1.00[YRI][hapmap] |
| rs2798179 | 1.00[YRI][hapmap] |
| rs5937892 | 1.00[YRI][hapmap] |
| rs5981301 | 1.00[YRI][hapmap] |
| rs5981692 | 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 | nsv916758 | chrX:73546406-74420929 | Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
