Variant report
Variant | rs9705599 |
---|---|
Chromosome Location | chr2:56548721-56548722 |
allele | G/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] |
---|---|
rs11829122 | 0.80[AFR][1000 genomes] |
rs11829680 | 0.80[AFR][1000 genomes] |
rs11830228 | 0.80[AFR][1000 genomes] |
rs11830290 | 0.80[AFR][1000 genomes] |
rs11830441 | 0.80[AFR][1000 genomes] |
rs11830677 | 0.80[AFR][1000 genomes] |
rs11831245 | 0.80[AFR][1000 genomes] |
rs11831251 | 0.80[AFR][1000 genomes] |
rs11831293 | 0.80[AFR][1000 genomes] |
rs11831349 | 0.80[AFR][1000 genomes] |
rs11831993 | 0.80[AFR][1000 genomes] |
rs11832032 | 0.80[AFR][1000 genomes] |
rs11833361 | 0.80[AFR][1000 genomes] |
rs11833447 | 0.83[AFR][1000 genomes] |
rs11833485 | 0.80[AFR][1000 genomes] |
rs11833642 | 0.80[AFR][1000 genomes] |
rs11834567 | 0.80[AFR][1000 genomes] |
rs11834927 | 0.80[AFR][1000 genomes] |
rs11835144 | 0.80[AFR][1000 genomes] |
rs11835169 | 0.80[AFR][1000 genomes] |
rs11835519 | 0.83[AFR][1000 genomes] |
rs11835895 | 0.80[AFR][1000 genomes] |
rs11835906 | 0.80[AFR][1000 genomes] |
rs11836005 | 0.80[AFR][1000 genomes] |
rs11836137 | 0.80[AFR][1000 genomes] |
rs11836718 | 0.80[AFR][1000 genomes] |
rs11837063 | 0.80[AFR][1000 genomes] |
rs11837134 | 0.80[AFR][1000 genomes] |
rs11837278 | 0.80[AFR][1000 genomes] |
rs11837438 | 0.80[AFR][1000 genomes] |
rs11837446 | 0.80[AFR][1000 genomes] |
rs11837623 | 0.80[AFR][1000 genomes] |
rs11837884 | 0.80[AFR][1000 genomes] |
rs11837915 | 0.80[AFR][1000 genomes] |
rs11838172 | 0.80[AFR][1000 genomes] |
rs12099627 | 0.80[AFR][1000 genomes] |
rs12099659 | 0.80[AFR][1000 genomes] |
rs12819568 | 0.80[AFR][1000 genomes] |
rs55657497 | 0.80[AFR][1000 genomes] |
rs55681645 | 0.80[AFR][1000 genomes] |
rs55703132 | 0.80[AFR][1000 genomes] |
rs55714406 | 0.80[AFR][1000 genomes] |
rs55877562 | 0.80[AFR][1000 genomes] |
rs55952122 | 0.80[AFR][1000 genomes] |
rs55959478 | 0.80[AFR][1000 genomes] |
rs55967587 | 0.80[AFR][1000 genomes] |
rs56049789 | 0.80[AFR][1000 genomes] |
rs56071884 | 0.80[AFR][1000 genomes] |
rs56090635 | 0.80[AFR][1000 genomes] |
rs56094917 | 0.80[AFR][1000 genomes] |
rs56098132 | 0.80[AFR][1000 genomes] |
rs56120992 | 0.80[AFR][1000 genomes] |
rs56150499 | 0.80[AFR][1000 genomes] |
rs56159241 | 0.80[AFR][1000 genomes] |
rs56177546 | 0.80[AFR][1000 genomes] |
rs56188823 | 0.80[AFR][1000 genomes] |
rs56205928 | 0.80[AFR][1000 genomes] |
rs56207554 | 0.80[AFR][1000 genomes] |
rs56237318 | 0.80[AFR][1000 genomes] |
rs56242467 | 0.80[AFR][1000 genomes] |
rs56314587 | 0.80[AFR][1000 genomes] |
rs56361480 | 0.80[AFR][1000 genomes] |
rs56391397 | 0.80[AFR][1000 genomes] |
rs56409370 | 0.80[AFR][1000 genomes] |
rs56412601 | 0.80[AFR][1000 genomes] |
rs56715199 | 0.80[AFR][1000 genomes] |
rs56724983 | 0.80[AFR][1000 genomes] |
rs56748402 | 0.80[AFR][1000 genomes] |
rs56768224 | 0.80[AFR][1000 genomes] |
rs56837577 | 0.80[AFR][1000 genomes] |
rs56909132 | 0.80[AFR][1000 genomes] |
rs56965441 | 0.80[AFR][1000 genomes] |
rs57081134 | 0.80[AFR][1000 genomes] |
rs57260754 | 0.80[AFR][1000 genomes] |
rs57371390 | 0.80[AFR][1000 genomes] |
rs57610337 | 0.80[AFR][1000 genomes] |
rs57766387 | 0.80[AFR][1000 genomes] |
rs57875495 | 0.80[AFR][1000 genomes] |
rs58032451 | 0.80[AFR][1000 genomes] |
rs58044216 | 0.80[AFR][1000 genomes] |
rs58238273 | 0.80[AFR][1000 genomes] |
rs58301692 | 0.80[AFR][1000 genomes] |
rs58363858 | 0.80[AFR][1000 genomes] |
rs58370767 | 0.80[AFR][1000 genomes] |
rs58381871 | 0.80[AFR][1000 genomes] |
rs58386990 | 0.80[AFR][1000 genomes] |
rs58624224 | 0.80[AFR][1000 genomes] |
rs58729422 | 0.80[AFR][1000 genomes] |
rs58797991 | 0.80[AFR][1000 genomes] |
rs58879230 | 0.80[AFR][1000 genomes] |
rs58955776 | 0.80[AFR][1000 genomes] |
rs59420328 | 0.80[AFR][1000 genomes] |
rs59442403 | 0.80[AFR][1000 genomes] |
rs59480955 | 0.80[AFR][1000 genomes] |
rs59498608 | 0.80[AFR][1000 genomes] |
rs59556442 | 0.80[AFR][1000 genomes] |
rs59634197 | 0.80[AFR][1000 genomes] |
rs59823325 | 0.80[AFR][1000 genomes] |
rs59868168 | 0.80[AFR][1000 genomes] |
rs60174931 | 0.80[AFR][1000 genomes] |
rs60552369 | 0.80[AFR][1000 genomes] |
rs60686453 | 0.80[AFR][1000 genomes] |
rs60703540 | 0.80[AFR][1000 genomes] |
rs61250726 | 0.80[AFR][1000 genomes] |
rs61265571 | 0.80[AFR][1000 genomes] |
rs61324351 | 0.80[AFR][1000 genomes] |
rs61352041 | 0.80[AFR][1000 genomes] |
rs61411066 | 0.80[AFR][1000 genomes] |
rs61471632 | 0.80[AFR][1000 genomes] |
rs61565811 | 0.80[AFR][1000 genomes] |
rs61687260 | 0.80[AFR][1000 genomes] |
rs74074113 | 0.80[AFR][1000 genomes] |
rs74074118 | 0.80[AFR][1000 genomes] |
rs74074130 | 0.80[AFR][1000 genomes] |
rs74074132 | 0.80[AFR][1000 genomes] |
rs74074136 | 0.80[AFR][1000 genomes] |
rs74074142 | 0.80[AFR][1000 genomes] |
rs74074143 | 0.80[AFR][1000 genomes] |
rs74074145 | 0.80[AFR][1000 genomes] |
rs74074160 | 0.80[AFR][1000 genomes] |
rs74074164 | 0.80[AFR][1000 genomes] |
rs74074165 | 0.80[AFR][1000 genomes] |
rs74074173 | 0.80[AFR][1000 genomes] |
rs74074174 | 0.80[AFR][1000 genomes] |
rs74074178 | 0.80[AFR][1000 genomes] |
rs74074194 | 0.80[AFR][1000 genomes] |
rs74074199 | 0.80[AFR][1000 genomes] |
rs74074200 | 0.80[AFR][1000 genomes] |
rs74074212 | 0.80[AFR][1000 genomes] |
rs74075903 | 0.80[AFR][1000 genomes] |
rs74075911 | 0.80[AFR][1000 genomes] |
rs74075914 | 0.80[AFR][1000 genomes] |
rs74075919 | 0.80[AFR][1000 genomes] |
rs74075924 | 0.80[AFR][1000 genomes] |
rs74075926 | 0.80[AFR][1000 genomes] |
rs74075929 | 0.80[AFR][1000 genomes] |
rs74075977 | 0.80[AFR][1000 genomes] |
rs74075981 | 0.80[AFR][1000 genomes] |
rs74075988 | 0.80[AFR][1000 genomes] |
rs74075989 | 0.80[AFR][1000 genomes] |
rs74075992 | 0.80[AFR][1000 genomes] |
rs74075994 | 0.80[AFR][1000 genomes] |
rs74075995 | 0.80[AFR][1000 genomes] |
rs74077249 | 0.80[AFR][1000 genomes] |
rs74077256 | 0.80[AFR][1000 genomes] |
rs74077323 | 0.83[AFR][1000 genomes] |
rs74077325 | 0.83[AFR][1000 genomes] |
rs74077334 | 0.83[AFR][1000 genomes] |
rs74077337 | 0.80[AFR][1000 genomes] |
rs74077343 | 0.83[AFR][1000 genomes] |
rs74077351 | 0.80[AFR][1000 genomes] |
rs74077358 | 0.80[AFR][1000 genomes] |
rs74077359 | 0.80[AFR][1000 genomes] |
rs74077360 | 0.80[AFR][1000 genomes] |
rs74077603 | 0.80[AFR][1000 genomes] |
rs74077604 | 0.80[AFR][1000 genomes] |
rs74077606 | 0.80[AFR][1000 genomes] |
rs74077607 | 0.80[AFR][1000 genomes] |
rs74077617 | 0.80[AFR][1000 genomes] |
rs74077621 | 0.80[AFR][1000 genomes] |
rs74077622 | 0.80[AFR][1000 genomes] |
rs74077625 | 0.80[AFR][1000 genomes] |
rs74077628 | 0.80[AFR][1000 genomes] |
rs74077630 | 0.80[AFR][1000 genomes] |
rs9705699 | 0.80[AFR][1000 genomes] |
rs9705808 | 0.80[AFR][1000 genomes] |
rs9705830 | 0.80[AFR][1000 genomes] |
rs9705863 | 0.80[AFR][1000 genomes] |
rs9706028 | 0.80[AFR][1000 genomes] |
rs9706487 | 1.00[AFR][1000 genomes] |
rs9706488 | 1.00[AFR][1000 genomes] |
rs9706494 | 0.80[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530516 | chr2:56447922-56633505 | Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
2 | nsv874170 | chr2:56496589-56590865 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv834093 | chr2:56538097-56708677 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv1004449 | chr2:56538460-56715861 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv874171 | chr2:56545845-56727178 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:56527600-56561000 | Weak transcription | HSMM | muscle |
2 | chr2:56546200-56552800 | Weak transcription | Left Ventricle | heart |