Variant report
| Variant | rs8010653 |
|---|---|
| Chromosome Location | chr14:79386707-79386708 |
| allele | A/G/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:8)
| rs_ID | r2[population] |
|---|---|
| rs11851757 | 0.85[JPT][hapmap] |
| rs31416 | 0.85[JPT][hapmap] |
| rs31423 | 0.82[ASN][1000 genomes] |
| rs31438 | 0.93[ASN][1000 genomes] |
| rs3805719 | 1.00[JPT][hapmap] |
| rs61995264 | 0.88[ASN][1000 genomes] |
| rs61995266 | 0.82[ASN][1000 genomes] |
| rs7160771 | 0.85[JPT][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 | nsv832838 | chr14:79306627-79445382 | Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
| 2 | nsv1048274 | chr14:79323592-79417906 | Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
