Variant report
| Variant | rs11761226 |
|---|---|
| Chromosome Location | chr7:14437084-14437085 |
| 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:28)
| rs_ID | r2[population] |
|---|---|
| rs10239634 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs10242478 | 0.94[AMR][1000 genomes] |
| rs10258060 | 1.00[YRI][hapmap] |
| rs10267135 | 0.94[AMR][1000 genomes] |
| rs10950523 | 1.00[JPT][hapmap] |
| rs10950524 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12666188 | 0.94[AMR][1000 genomes] |
| rs12668508 | 0.94[AMR][1000 genomes] |
| rs12671101 | 1.00[EUR][1000 genomes] |
| rs171927 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs196747 | 0.94[AMR][1000 genomes] |
| rs196749 | 0.86[JPT][hapmap];0.82[AMR][1000 genomes] |
| rs196752 | 0.82[JPT][hapmap];0.84[AMR][1000 genomes] |
| rs196754 | 0.82[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs196759 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs196763 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2060159 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes] |
| rs2060161 | 0.86[CHB][hapmap];0.88[JPT][hapmap];0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs4721333 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6461095 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
| rs6461098 | 0.85[CHB][hapmap];1.00[JPT][hapmap] |
| rs6971925 | 0.85[CHB][hapmap];1.00[JPT][hapmap] |
| rs73282311 | 0.94[AMR][1000 genomes] |
| rs73282318 | 0.94[AMR][1000 genomes] |
| rs73282321 | 0.94[AMR][1000 genomes] |
| rs73285809 | 0.88[AMR][1000 genomes] |
| rs7782300 | 0.86[AMR][1000 genomes] |
| rs969596 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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 | nsv949033 | chr7:14086106-14860323 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| 2 | nsv606281 | chr7:14388381-14443963 | Weak transcription Flanking Active TSS Enhancers Active TSS | n/a | n/a | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
