Variant report
Variant | rs2896760 |
---|---|
Chromosome Location | chr21:17858989-17858990 |
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] |
rs10470096 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs10470198 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10470199 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10470200 | 0.88[ASN][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] |
rs13433398 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs13433444 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs2039242 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs2039243 | 1.00[ASN][1000 genomes] |
rs2039244 | 1.00[ASN][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] |
rs2823832 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs2823833 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs2823834 | 1.00[EUR][1000 genomes] |
rs2823835 | 1.00[EUR][1000 genomes] |
rs2823836 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs2823837 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][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] |
rs2823878 | 1.00[JPT][hapmap] |
rs28407677 | 0.82[ASN][1000 genomes] |
rs28415058 | 1.00[ASN][1000 genomes] |
rs28433186 | 1.00[ASN][1000 genomes] |
rs28496427 | 1.00[EUR][1000 genomes] |
rs28526796 | 1.00[ASN][1000 genomes] |
rs28608983 | 1.00[ASN][1000 genomes] |
rs28643005 | 1.00[ASN][1000 genomes] |
rs28648637 | 1.00[ASN][1000 genomes] |
rs28690432 | 1.00[ASN][1000 genomes] |
rs28840743 | 0.88[ASN][1000 genomes] |
rs28844023 | 0.82[ASN][1000 genomes] |
rs28858813 | 0.88[ASN][1000 genomes] |
rs28875621 | 1.00[EUR][1000 genomes] |
rs28896613 | 0.82[ASN][1000 genomes] |
rs2896759 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57055406 | 0.88[ASN][1000 genomes] |
rs57523013 | 1.00[EUR][1000 genomes] |
rs57659737 | 0.88[ASN][1000 genomes] |
rs58072187 | 1.00[EUR][1000 genomes] |
rs58175294 | 1.00[EUR][1000 genomes] |
rs58225448 | 1.00[ASN][1000 genomes] |
rs58236716 | 1.00[ASN][1000 genomes] |
rs58304651 | 1.00[EUR][1000 genomes] |
rs58640456 | 1.00[EUR][1000 genomes] |
rs59959567 | 0.88[ASN][1000 genomes] |
rs60754236 | 1.00[EUR][1000 genomes] |
rs60925168 | 0.88[ASN][1000 genomes] |
rs61549904 | 1.00[ASN][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] |
rs73363406 | 1.00[EUR][1000 genomes] |
rs73363409 | 1.00[EUR][1000 genomes] |
rs73363411 | 1.00[EUR][1000 genomes] |
rs73363422 | 0.88[ASN][1000 genomes] |
rs73363426 | 0.88[ASN][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] |
rs73380342 | 1.00[ASN][1000 genomes] |
rs73380344 | 1.00[EUR][1000 genomes] |
rs73891591 | 1.00[ASN][1000 genomes] |
rs73891592 | 1.00[ASN][1000 genomes] |
rs73893713 | 1.00[ASN][1000 genomes] |
rs8128684 | 1.00[EUR][1000 genomes] |
rs8132608 | 1.00[EUR][1000 genomes] |
rs8132951 | 1.00[EUR][1000 genomes] |
rs8132964 | 1.00[ASN][1000 genomes] |
rs8133408 | 1.00[EUR][1000 genomes] |
rs8134501 | 1.00[EUR][1000 genomes] |
rs9305766 | 1.00[JPT][hapmap];0.88[ASN][1000 genomes] |
rs9305767 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9305768 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9305769 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs9305773 | 1.00[EUR][1000 genomes] |
rs9974386 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9974447 | 0.82[ASN][1000 genomes] |
rs9974519 | 1.00[ASN][1000 genomes] |
rs9975047 | 0.88[ASN][1000 genomes] |
rs9975202 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9975349 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs9975582 | 0.88[ASN][1000 genomes] |
rs9975640 | 1.00[ASN][1000 genomes] |
rs9976077 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9976320 | 1.00[EUR][1000 genomes] |
rs9976648 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9976683 | 1.00[EUR][1000 genomes] |
rs9976729 | 0.82[ASN][1000 genomes] |
rs9976887 | 1.00[ASN][1000 genomes] |
rs9977372 | 0.88[ASN][1000 genomes] |
rs9977640 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9977666 | 0.82[ASN][1000 genomes] |
rs9977870 | 1.00[EUR][1000 genomes] |
rs9978828 | 1.00[ASN][1000 genomes] |
rs9979222 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9979766 | 0.88[ASN][1000 genomes] |
rs9979904 | 0.88[ASN][1000 genomes] |
rs9980133 | 1.00[ASN][1000 genomes] |
rs9980149 | 0.94[ASN][1000 genomes] |
rs9980549 | 0.82[ASN][1000 genomes] |
rs9980810 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9980959 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9981432 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9981465 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs9981475 | 1.00[EUR][1000 genomes] |
rs9981657 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9981699 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9982188 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9982511 | 1.00[ASN][1000 genomes] |
rs9982641 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9982850 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs9983223 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9983295 | 1.00[ASN][1000 genomes] |
rs9983298 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9983466 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9984183 | 1.00[ASN][1000 genomes] |
rs9984263 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9984639 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes] |
rs9984788 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9985004 | 1.00[ASN][1000 genomes] |
rs9985090 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs9985151 | 0.88[ASN][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 | chr21:17849000-17863000 | Weak transcription | Liver | Liver |
6 | chr21:17858000-17866200 | Weak transcription | Left Ventricle | heart |
7 | chr21:17858400-17862200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
8 | chr21:17858400-17865000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
9 | chr21:17858600-17859400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
10 | chr21:17858600-17860800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
11 | chr21:17858800-17868000 | Weak transcription | Fetal Brain Female | brain |