Variant report
| Variant | rs11994160 |
|---|---|
| Chromosome Location | chr8:34353811-34353812 |
| 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:34)
| rs_ID | r2[population] |
|---|---|
| rs10089410 | 1.00[ASN][1000 genomes] |
| rs10092484 | 1.00[ASN][1000 genomes] |
| rs10099704 | 1.00[ASN][1000 genomes] |
| rs10099911 | 1.00[ASN][1000 genomes] |
| rs10100213 | 1.00[ASN][1000 genomes] |
| rs10108508 | 1.00[ASN][1000 genomes] |
| rs10111870 | 1.00[ASN][1000 genomes] |
| rs10217066 | 1.00[ASN][1000 genomes] |
| rs12334566 | 1.00[ASN][1000 genomes] |
| rs16882055 | 1.00[ASN][1000 genomes] |
| rs16882266 | 1.00[ASN][1000 genomes] |
| rs16882365 | 1.00[ASN][1000 genomes] |
| rs16882528 | 1.00[ASN][1000 genomes] |
| rs16882705 | 1.00[ASN][1000 genomes] |
| rs2719272 | 1.00[ASN][1000 genomes] |
| rs28505609 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs35112066 | 1.00[ASN][1000 genomes] |
| rs6468269 | 1.00[ASN][1000 genomes] |
| rs67406212 | 1.00[ASN][1000 genomes] |
| rs67908341 | 1.00[ASN][1000 genomes] |
| rs6988783 | 1.00[ASN][1000 genomes] |
| rs7000467 | 1.00[ASN][1000 genomes] |
| rs7009639 | 1.00[ASN][1000 genomes] |
| rs71513723 | 1.00[ASN][1000 genomes] |
| rs72629509 | 1.00[ASN][1000 genomes] |
| rs72629510 | 1.00[ASN][1000 genomes] |
| rs72640903 | 1.00[ASN][1000 genomes] |
| rs72640915 | 1.00[ASN][1000 genomes] |
| rs72640931 | 1.00[ASN][1000 genomes] |
| rs72640933 | 1.00[ASN][1000 genomes] |
| rs72640961 | 1.00[ASN][1000 genomes] |
| rs72640962 | 1.00[ASN][1000 genomes] |
| rs72644259 | 1.00[ASN][1000 genomes] |
| rs7815445 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
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 | nsv6147 | chr8:34314029-34359124 | Weak transcription Enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:34351400-34356200 | Weak transcription | Fetal Heart | heart |
