Variant report
Variant | rs11006577 |
---|---|
Chromosome Location | chr10:61324299-61324300 |
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] |
---|---|
rs10458677 | 0.83[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs10509108 | 0.83[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs10740776 | 0.96[ASN][1000 genomes] |
rs10826320 | 0.83[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs10826321 | 0.83[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs10826324 | 0.97[ASN][1000 genomes] |
rs10826325 | 0.96[ASN][1000 genomes] |
rs11006586 | 0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11006589 | 0.81[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs11006593 | 0.97[ASN][1000 genomes] |
rs11006605 | 0.94[ASN][1000 genomes] |
rs12217745 | 0.97[ASN][1000 genomes] |
rs12218834 | 0.97[ASN][1000 genomes] |
rs12268265 | 0.95[ASN][1000 genomes] |
rs12570492 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs4341489 | 0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs56299211 | 0.84[EUR][1000 genomes] |
rs61862307 | 0.95[ASN][1000 genomes] |
rs7087413 | 0.97[ASN][1000 genomes] |
rs7099911 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv895564 | chr10:61220923-61327502 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv551150 | chr10:61286904-61330297 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | esv3693063 | chr10:61316344-61331087 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | esv2757394 | chr10:61324135-61333139 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv2759762 | chr10:61324135-61333139 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:61323800-61324400 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |