Variant report
| Variant | rs7317093 |
|---|---|
| Chromosome Location | chr13:88538762-88538763 |
| 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:27)
| rs_ID | r2[population] |
|---|---|
| rs16962286 | 1.00[AMR][1000 genomes] |
| rs16963883 | 1.00[AMR][1000 genomes] |
| rs16964065 | 1.00[AMR][1000 genomes] |
| rs2184536 | 1.00[AMR][1000 genomes] |
| rs56248013 | 1.00[AMR][1000 genomes] |
| rs58185871 | 1.00[AMR][1000 genomes] |
| rs58386677 | 1.00[AMR][1000 genomes] |
| rs59150082 | 1.00[AMR][1000 genomes] |
| rs59917522 | 1.00[AMR][1000 genomes] |
| rs60620898 | 1.00[AMR][1000 genomes] |
| rs6491604 | 1.00[AMR][1000 genomes] |
| rs73565306 | 1.00[AMR][1000 genomes] |
| rs73565308 | 1.00[AMR][1000 genomes] |
| rs73565313 | 1.00[AMR][1000 genomes] |
| rs73565336 | 1.00[AMR][1000 genomes] |
| rs73580563 | 1.00[AMR][1000 genomes] |
| rs74103986 | 1.00[AMR][1000 genomes] |
| rs74103987 | 1.00[AMR][1000 genomes] |
| rs74104001 | 1.00[AMR][1000 genomes] |
| rs74104429 | 1.00[AMR][1000 genomes] |
| rs74104436 | 1.00[AMR][1000 genomes] |
| rs74104437 | 1.00[AMR][1000 genomes] |
| rs74104452 | 1.00[AMR][1000 genomes] |
| rs74106810 | 1.00[AMR][1000 genomes] |
| rs74106811 | 1.00[AMR][1000 genomes] |
| rs74106812 | 1.00[AMR][1000 genomes] |
| rs7985798 | 1.00[AMR][1000 genomes] |
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 | nsv832673 | chr13:88431110-88607319 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| 2 | nsv562632 | chr13:88532287-88622740 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:88538200-88539800 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
