Variant report
Variant | rs9349726 |
---|---|
Chromosome Location | chr6:54490041-54490042 |
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] |
---|---|
rs1039495 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1039496 | 0.80[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10948839 | 0.85[ASN][1000 genomes] |
rs10948840 | 0.92[EUR][1000 genomes] |
rs11966577 | 0.85[ASN][1000 genomes] |
rs12525539 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12527077 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs12527080 | 0.90[EUR][1000 genomes] |
rs12527124 | 0.90[EUR][1000 genomes] |
rs12527767 | 0.87[ASN][1000 genomes] |
rs12528270 | 0.90[EUR][1000 genomes] |
rs12528881 | 0.90[EUR][1000 genomes] |
rs12529275 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12662465 | 0.90[EUR][1000 genomes] |
rs1395624 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1395627 | 0.81[ASN][1000 genomes] |
rs1648200 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs1648201 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs16869519 | 0.87[EUR][1000 genomes] |
rs16885649 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs16885654 | 0.87[ASN][1000 genomes] |
rs16885656 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs16885668 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs16885735 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs16885760 | 0.81[ASN][1000 genomes] |
rs16885866 | 0.92[EUR][1000 genomes] |
rs16885948 | 0.82[EUR][1000 genomes] |
rs1745079 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs1951693 | 0.87[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs1976539 | 0.91[EUR][1000 genomes] |
rs2048112 | 0.92[EUR][1000 genomes] |
rs2894821 | 0.81[EUR][1000 genomes] |
rs34659714 | 0.85[ASN][1000 genomes] |
rs34752465 | 0.92[EUR][1000 genomes] |
rs4712065 | 0.81[ASN][1000 genomes] |
rs4712066 | 0.81[ASN][1000 genomes] |
rs4712068 | 0.90[EUR][1000 genomes] |
rs4715466 | 0.85[ASN][1000 genomes] |
rs4715468 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4715470 | 0.90[EUR][1000 genomes] |
rs4994100 | 0.81[EUR][1000 genomes] |
rs541689 | 0.90[ASN][1000 genomes] |
rs58302712 | 0.80[EUR][1000 genomes] |
rs60501416 | 0.80[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs608873 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs61375854 | 0.81[ASN][1000 genomes] |
rs6915244 | 0.82[EUR][1000 genomes] |
rs73440097 | 0.81[ASN][1000 genomes] |
rs73444113 | 0.89[EUR][1000 genomes] |
rs73444116 | 0.90[EUR][1000 genomes] |
rs73444125 | 0.89[EUR][1000 genomes] |
rs73446030 | 0.82[EUR][1000 genomes] |
rs73446036 | 0.82[EUR][1000 genomes] |
rs73446043 | 0.82[EUR][1000 genomes] |
rs7450207 | 0.84[ASN][1000 genomes] |
rs7740110 | 0.81[ASN][1000 genomes] |
rs7751908 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7753964 | 0.89[ASN][1000 genomes] |
rs7761021 | 0.92[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7766941 | 0.90[ASN][1000 genomes] |
rs9370323 | 0.86[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs9474957 | 0.83[EUR][1000 genomes] |
rs950077 | 0.85[ASN][1000 genomes] |
rs953896 | 0.85[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv427757 | chr6:54296552-54507210 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv981146 | chr6:54487057-54496676 | Weak transcription Enhancers | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:54489000-54490800 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
2 | chr6:54489200-54490400 | Enhancers | Osteobl | bone |
3 | chr6:54489600-54490200 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |