Variant report
Variant | rs73363406 |
---|---|
Chromosome Location | chr21:17850344-17850345 |
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 |
rs_ID | r2[population] |
---|---|
rs10084567 | 1.00[EUR][1000 genomes] |
rs10084608 | 1.00[EUR][1000 genomes] |
rs10084612 | 1.00[EUR][1000 genomes] |
rs12482215 | 1.00[EUR][1000 genomes] |
rs12482914 | 1.00[EUR][1000 genomes] |
rs12483358 | 1.00[EUR][1000 genomes] |
rs12483622 | 1.00[EUR][1000 genomes] |
rs2040142 | 1.00[EUR][1000 genomes] |
rs2212562 | 1.00[EUR][1000 genomes] |
rs2226435 | 1.00[EUR][1000 genomes] |
rs2823821 | 1.00[EUR][1000 genomes] |
rs2823822 | 1.00[EUR][1000 genomes] |
rs2823825 | 1.00[EUR][1000 genomes] |
rs2823826 | 1.00[EUR][1000 genomes] |
rs2823827 | 1.00[EUR][1000 genomes] |
rs2823828 | 1.00[EUR][1000 genomes] |
rs2823830 | 1.00[EUR][1000 genomes] |
rs2823831 | 1.00[EUR][1000 genomes] |
rs2823834 | 1.00[EUR][1000 genomes] |
rs2823835 | 1.00[EUR][1000 genomes] |
rs2823853 | 1.00[EUR][1000 genomes] |
rs2823854 | 1.00[EUR][1000 genomes] |
rs2823855 | 1.00[EUR][1000 genomes] |
rs2823860 | 1.00[EUR][1000 genomes] |
rs2823866 | 1.00[EUR][1000 genomes] |
rs28496427 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28840743 | 1.00[AMR][1000 genomes] |
rs28875621 | 1.00[EUR][1000 genomes] |
rs2896759 | 1.00[EUR][1000 genomes] |
rs2896760 | 1.00[EUR][1000 genomes] |
rs57055406 | 1.00[AMR][1000 genomes] |
rs57523013 | 1.00[EUR][1000 genomes] |
rs57659737 | 1.00[AMR][1000 genomes] |
rs58072187 | 1.00[EUR][1000 genomes] |
rs58175294 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58304651 | 1.00[EUR][1000 genomes] |
rs58640456 | 1.00[EUR][1000 genomes] |
rs59959567 | 0.83[AMR][1000 genomes] |
rs60754236 | 1.00[EUR][1000 genomes] |
rs60925168 | 1.00[AMR][1000 genomes] |
rs7277815 | 1.00[EUR][1000 genomes] |
rs7278273 | 1.00[EUR][1000 genomes] |
rs7280438 | 1.00[EUR][1000 genomes] |
rs7283241 | 1.00[EUR][1000 genomes] |
rs7283307 | 1.00[EUR][1000 genomes] |
rs7283311 | 1.00[EUR][1000 genomes] |
rs73363409 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73363411 | 1.00[EUR][1000 genomes] |
rs73363422 | 1.00[AMR][1000 genomes] |
rs73363426 | 1.00[AMR][1000 genomes] |
rs73366681 | 1.00[EUR][1000 genomes] |
rs73366695 | 1.00[EUR][1000 genomes] |
rs73368504 | 1.00[EUR][1000 genomes] |
rs73368506 | 1.00[EUR][1000 genomes] |
rs73368523 | 1.00[EUR][1000 genomes] |
rs73380344 | 1.00[EUR][1000 genomes] |
rs8128684 | 1.00[EUR][1000 genomes] |
rs8132608 | 1.00[EUR][1000 genomes] |
rs8132951 | 1.00[EUR][1000 genomes] |
rs8133408 | 1.00[EUR][1000 genomes] |
rs8134501 | 1.00[EUR][1000 genomes] |
rs9305773 | 1.00[EUR][1000 genomes] |
rs9976320 | 1.00[EUR][1000 genomes] |
rs9976683 | 1.00[EUR][1000 genomes] |
rs9977372 | 0.83[AMR][1000 genomes] |
rs9977870 | 1.00[EUR][1000 genomes] |
rs9981475 | 1.00[EUR][1000 genomes] |
rs9984639 | 1.00[AMR][1000 genomes] |
rs9984970 | 0.83[AMR][1000 genomes] |
rs9985151 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1064857 | chr21:17628760-18533131 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 345 gene(s) | inside rSNPs | diseases |
2 | nsv544382 | chr21:17628760-18533131 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 345 gene(s) | inside rSNPs | diseases |
3 | nsv913416 | chr21:17728224-17863882 | Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:17840400-17860800 | Weak transcription | HUVEC | blood vessel |
2 | chr21:17841000-17881800 | Weak transcription | Hela-S3 | cervix |
3 | chr21:17846600-17859400 | Weak transcription | Ovary | ovary |
4 | chr21:17846800-17864000 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
5 | chr21:17849000-17851800 | Weak transcription | Muscle Satellite Cultured Cells | -- |
6 | chr21:17849000-17863000 | Weak transcription | Liver | Liver |
7 | chr21:17850200-17850800 | ZNF genes & repeats | H9 Derived Neuron Cultured Cells | ES cell derived |