Variant report
Variant | rs9928252 |
---|---|
Chromosome Location | chr16:80674641-80674642 |
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] |
---|---|
rs1109548 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1121650 | 1.00[EUR][1000 genomes] |
rs1121652 | 1.00[EUR][1000 genomes] |
rs13329835 | 0.90[ASN][1000 genomes] |
rs13330440 | 1.00[EUR][1000 genomes] |
rs13330445 | 1.00[EUR][1000 genomes] |
rs13330499 | 1.00[EUR][1000 genomes] |
rs13330767 | 1.00[EUR][1000 genomes] |
rs13330810 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs13331630 | 1.00[EUR][1000 genomes] |
rs13331892 | 1.00[EUR][1000 genomes] |
rs13331986 | 1.00[EUR][1000 genomes] |
rs13332868 | 1.00[EUR][1000 genomes] |
rs13333408 | 1.00[EUR][1000 genomes] |
rs13333588 | 1.00[EUR][1000 genomes] |
rs13333733 | 1.00[EUR][1000 genomes] |
rs13334543 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13334600 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13335334 | 1.00[EUR][1000 genomes] |
rs13335525 | 1.00[EUR][1000 genomes] |
rs13335681 | 1.00[EUR][1000 genomes] |
rs13336185 | 1.00[EUR][1000 genomes] |
rs13336514 | 1.00[EUR][1000 genomes] |
rs13336555 | 1.00[EUR][1000 genomes] |
rs13336721 | 1.00[EUR][1000 genomes] |
rs13336748 | 1.00[EUR][1000 genomes] |
rs13336757 | 1.00[EUR][1000 genomes] |
rs13336797 | 1.00[EUR][1000 genomes] |
rs13337893 | 1.00[EUR][1000 genomes] |
rs13338430 | 1.00[EUR][1000 genomes] |
rs13339031 | 1.00[EUR][1000 genomes] |
rs1982420 | 0.90[ASN][1000 genomes] |
rs2167671 | 0.90[ASN][1000 genomes] |
rs28435276 | 1.00[EUR][1000 genomes] |
rs28439236 | 1.00[EUR][1000 genomes] |
rs28453876 | 1.00[EUR][1000 genomes] |
rs28484999 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs28600122 | 1.00[EUR][1000 genomes] |
rs28629992 | 1.00[EUR][1000 genomes] |
rs28637533 | 1.00[EUR][1000 genomes] |
rs28641984 | 1.00[EUR][1000 genomes] |
rs28758756 | 1.00[EUR][1000 genomes] |
rs28758801 | 1.00[EUR][1000 genomes] |
rs28773800 | 1.00[EUR][1000 genomes] |
rs28846148 | 1.00[EUR][1000 genomes] |
rs28847920 | 1.00[EUR][1000 genomes] |
rs28860586 | 1.00[EUR][1000 genomes] |
rs28872224 | 1.00[EUR][1000 genomes] |
rs56009700 | 1.00[EUR][1000 genomes] |
rs56096652 | 1.00[EUR][1000 genomes] |
rs56301423 | 1.00[EUR][1000 genomes] |
rs57865804 | 1.00[EUR][1000 genomes] |
rs59272180 | 1.00[EUR][1000 genomes] |
rs60851276 | 1.00[EUR][1000 genomes] |
rs7187578 | 1.00[EUR][1000 genomes] |
rs7189369 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7194867 | 1.00[EUR][1000 genomes] |
rs7201458 | 1.00[EUR][1000 genomes] |
rs7201468 | 1.00[EUR][1000 genomes] |
rs7206878 | 1.00[EUR][1000 genomes] |
rs73583632 | 1.00[EUR][1000 genomes] |
rs73583633 | 1.00[EUR][1000 genomes] |
rs73583634 | 1.00[EUR][1000 genomes] |
rs73583636 | 1.00[EUR][1000 genomes] |
rs73583637 | 1.00[EUR][1000 genomes] |
rs73583639 | 1.00[EUR][1000 genomes] |
rs73583641 | 1.00[EUR][1000 genomes] |
rs73583645 | 1.00[EUR][1000 genomes] |
rs73592214 | 1.00[EUR][1000 genomes] |
rs73592230 | 1.00[EUR][1000 genomes] |
rs73592249 | 1.00[EUR][1000 genomes] |
rs73592251 | 1.00[EUR][1000 genomes] |
rs73592252 | 1.00[EUR][1000 genomes] |
rs73592253 | 1.00[EUR][1000 genomes] |
rs73592254 | 1.00[EUR][1000 genomes] |
rs73592255 | 1.00[EUR][1000 genomes] |
rs74028340 | 1.00[EUR][1000 genomes] |
rs74028351 | 1.00[EUR][1000 genomes] |
rs74028355 | 1.00[EUR][1000 genomes] |
rs74028361 | 1.00[EUR][1000 genomes] |
rs74028362 | 1.00[EUR][1000 genomes] |
rs74028365 | 1.00[EUR][1000 genomes] |
rs8056731 | 0.90[ASN][1000 genomes] |
rs8060464 | 1.00[EUR][1000 genomes] |
rs8061127 | 1.00[EUR][1000 genomes] |
rs873994 | 0.90[ASN][1000 genomes] |
rs879843 | 0.90[ASN][1000 genomes] |
rs9921238 | 1.00[EUR][1000 genomes] |
rs9921314 | 1.00[EUR][1000 genomes] |
rs9922776 | 1.00[EUR][1000 genomes] |
rs9923568 | 1.00[EUR][1000 genomes] |
rs9923974 | 1.00[EUR][1000 genomes] |
rs9924545 | 1.00[EUR][1000 genomes] |
rs9927905 | 1.00[EUR][1000 genomes] |
rs9928159 | 1.00[EUR][1000 genomes] |
rs9928160 | 1.00[EUR][1000 genomes] |
rs9928723 | 1.00[EUR][1000 genomes] |
rs9929914 | 1.00[EUR][1000 genomes] |
rs9930172 | 1.00[EUR][1000 genomes] |
rs9930510 | 1.00[EUR][1000 genomes] |
rs9930675 | 1.00[EUR][1000 genomes] |
rs9931563 | 1.00[EUR][1000 genomes] |
rs9931732 | 1.00[EUR][1000 genomes] |
rs9932584 | 1.00[EUR][1000 genomes] |
rs9933028 | 1.00[EUR][1000 genomes] |
rs9933317 | 1.00[EUR][1000 genomes] |
rs9933575 | 1.00[EUR][1000 genomes] |
rs9935562 | 1.00[EUR][1000 genomes] |
rs9936109 | 1.00[EUR][1000 genomes] |
rs9936704 | 1.00[EUR][1000 genomes] |
rs9938384 | 1.00[EUR][1000 genomes] |
rs9939159 | 1.00[EUR][1000 genomes] |
rs9939945 | 1.00[EUR][1000 genomes] |
rs9939967 | 1.00[EUR][1000 genomes] |
rs9940133 | 1.00[EUR][1000 genomes] |
rs9940999 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1060621 | chr16:80532848-80980616 | Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
2 | nsv542989 | chr16:80532848-80980616 | Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
3 | nsv1057562 | chr16:80650768-80675842 | Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1058764 | chr16:80656966-80707848 | Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv1057357 | chr16:80662770-80794945 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:80646600-80687800 | Weak transcription | Pancreas | Pancrea |
2 | chr16:80663200-80690200 | Weak transcription | Primary mononuclear cells fromperipheralblood | Blood |
3 | chr16:80664200-80675800 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
4 | chr16:80665400-80677200 | Weak transcription | Gastric | stomach |
5 | chr16:80667400-80675200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
6 | chr16:80667400-80690000 | Weak transcription | Spleen | Spleen |
7 | chr16:80671400-80676200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
8 | chr16:80674200-80675000 | Weak transcription | Aorta | Aorta |
9 | chr16:80674400-80687800 | Weak transcription | Hela-S3 | cervix |
10 | chr16:80674400-80707600 | Weak transcription | Placenta | Placenta |