Variant report
Variant | rs7005808 |
---|---|
Chromosome Location | chr8:34532101-34532102 |
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 |
rs_ID | r2[population] |
---|---|
rs10110457 | 0.84[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs11995347 | 0.81[AMR][1000 genomes] |
rs13260157 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13261872 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13262347 | 0.81[AMR][1000 genomes] |
rs13268340 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1403377 | 0.81[AMR][1000 genomes] |
rs1522849 | 0.81[AMR][1000 genomes] |
rs1522850 | 0.81[AMR][1000 genomes] |
rs1608233 | 0.88[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs1916172 | 0.81[AMR][1000 genomes] |
rs1916176 | 0.81[AMR][1000 genomes] |
rs1949719 | 0.81[AMR][1000 genomes] |
rs1949720 | 0.81[AMR][1000 genomes] |
rs2685591 | 0.81[AMR][1000 genomes] |
rs2685599 | 0.81[AMR][1000 genomes] |
rs2685607 | 0.81[AMR][1000 genomes] |
rs2687554 | 0.81[AMR][1000 genomes] |
rs2687556 | 0.81[AMR][1000 genomes] |
rs4556086 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6468286 | 0.81[AMR][1000 genomes] |
rs6994824 | 0.81[AMR][1000 genomes] |
rs7816776 | 0.84[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs7822537 | 0.88[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs7837402 | 0.88[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs7843303 | 0.81[AMR][1000 genomes] |
rs7845916 | 0.81[AMR][1000 genomes] |
rs952902 | 0.81[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv831283 | chr8:34501243-34662634 | Enhancers Weak transcription ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:34531600-34533000 | Enhancers | iPS-20b Cell Line | embryonic stem cell |