Variant report
Variant | rs12269643 |
---|---|
Chromosome Location | chr10:93209518-93209519 |
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] |
---|---|
rs11186558 | 0.93[ASN][1000 genomes] |
rs11186560 | 0.95[ASN][1000 genomes] |
rs11186565 | 0.98[ASN][1000 genomes] |
rs11186567 | 1.00[ASN][1000 genomes] |
rs11186570 | 1.00[ASN][1000 genomes] |
rs11186573 | 0.95[ASN][1000 genomes] |
rs11186574 | 0.95[ASN][1000 genomes] |
rs11186575 | 0.95[ASN][1000 genomes] |
rs11186580 | 0.95[ASN][1000 genomes] |
rs11186584 | 0.95[ASN][1000 genomes] |
rs11186585 | 0.95[ASN][1000 genomes] |
rs11186586 | 0.95[ASN][1000 genomes] |
rs11186595 | 0.95[ASN][1000 genomes] |
rs11186596 | 0.95[ASN][1000 genomes] |
rs11186597 | 0.95[ASN][1000 genomes] |
rs11186604 | 0.82[ASN][1000 genomes] |
rs11186605 | 0.84[ASN][1000 genomes] |
rs11186606 | 0.82[ASN][1000 genomes] |
rs11186607 | 0.91[ASN][1000 genomes] |
rs12240706 | 0.95[ASN][1000 genomes] |
rs12241174 | 0.87[ASN][1000 genomes] |
rs12242238 | 0.93[ASN][1000 genomes] |
rs12242257 | 1.00[ASN][1000 genomes] |
rs12242663 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs12242821 | 0.95[ASN][1000 genomes] |
rs12244155 | 0.82[ASN][1000 genomes] |
rs12245101 | 0.93[ASN][1000 genomes] |
rs12247442 | 0.95[ASN][1000 genomes] |
rs12247672 | 0.93[ASN][1000 genomes] |
rs12249854 | 1.00[ASN][1000 genomes] |
rs12250037 | 1.00[ASN][1000 genomes] |
rs12253137 | 0.95[ASN][1000 genomes] |
rs12253556 | 0.93[ASN][1000 genomes] |
rs12257663 | 0.95[ASN][1000 genomes] |
rs12258185 | 1.00[ASN][1000 genomes] |
rs12258439 | 0.95[ASN][1000 genomes] |
rs12259631 | 0.95[ASN][1000 genomes] |
rs12259834 | 0.95[ASN][1000 genomes] |
rs12261527 | 0.93[ASN][1000 genomes] |
rs12262057 | 0.93[ASN][1000 genomes] |
rs12263089 | 1.00[ASN][1000 genomes] |
rs12265269 | 0.95[ASN][1000 genomes] |
rs12266112 | 0.95[ASN][1000 genomes] |
rs12268013 | 0.95[ASN][1000 genomes] |
rs1329652 | 0.95[ASN][1000 genomes] |
rs13376715 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs13376868 | 1.00[ASN][1000 genomes] |
rs1360187 | 0.95[ASN][1000 genomes] |
rs17106645 | 0.93[ASN][1000 genomes] |
rs17106657 | 1.00[ASN][1000 genomes] |
rs2068866 | 0.95[ASN][1000 genomes] |
rs2421517 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4376822 | 0.95[ASN][1000 genomes] |
rs4415665 | 1.00[ASN][1000 genomes] |
rs4586060 | 0.82[ASN][1000 genomes] |
rs55718133 | 0.95[ASN][1000 genomes] |
rs55762845 | 0.87[ASN][1000 genomes] |
rs56097320 | 1.00[ASN][1000 genomes] |
rs57033814 | 0.93[ASN][1000 genomes] |
rs57159565 | 0.95[ASN][1000 genomes] |
rs57314370 | 0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs57988119 | 0.95[ASN][1000 genomes] |
rs57996677 | 0.93[ASN][1000 genomes] |
rs59198703 | 0.86[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs59758370 | 0.95[ASN][1000 genomes] |
rs60640820 | 0.93[ASN][1000 genomes] |
rs61346715 | 0.84[ASN][1000 genomes] |
rs61579794 | 0.95[ASN][1000 genomes] |
rs6583769 | 0.85[ASN][1000 genomes] |
rs6583770 | 0.87[ASN][1000 genomes] |
rs6583775 | 0.95[ASN][1000 genomes] |
rs6583776 | 0.95[ASN][1000 genomes] |
rs6583777 | 0.95[ASN][1000 genomes] |
rs7072087 | 0.95[ASN][1000 genomes] |
rs7074559 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs7075344 | 0.95[ASN][1000 genomes] |
rs7075424 | 0.95[ASN][1000 genomes] |
rs7076784 | 1.00[ASN][1000 genomes] |
rs7077014 | 1.00[ASN][1000 genomes] |
rs7077715 | 0.93[ASN][1000 genomes] |
rs7081363 | 0.85[ASN][1000 genomes] |
rs7085276 | 0.95[ASN][1000 genomes] |
rs7091647 | 0.91[ASN][1000 genomes] |
rs7100516 | 0.93[ASN][1000 genomes] |
rs73316210 | 0.93[ASN][1000 genomes] |
rs73316216 | 0.95[ASN][1000 genomes] |
rs73316246 | 0.95[ASN][1000 genomes] |
rs73316284 | 0.93[ASN][1000 genomes] |
rs7342052 | 1.00[ASN][1000 genomes] |
rs7478184 | 0.95[ASN][1000 genomes] |
rs7893331 | 0.93[ASN][1000 genomes] |
rs7893826 | 0.93[ASN][1000 genomes] |
rs7894248 | 0.95[ASN][1000 genomes] |
rs7895666 | 0.95[ASN][1000 genomes] |
rs7898769 | 0.95[ASN][1000 genomes] |
rs7898845 | 0.95[ASN][1000 genomes] |
rs7904917 | 0.95[ASN][1000 genomes] |
rs7905307 | 0.93[ASN][1000 genomes] |
rs7906306 | 1.00[ASN][1000 genomes] |
rs7906515 | 0.93[ASN][1000 genomes] |
rs7907010 | 0.95[ASN][1000 genomes] |
rs7907154 | 0.88[ASN][1000 genomes] |
rs7908457 | 0.95[ASN][1000 genomes] |
rs7908769 | 1.00[ASN][1000 genomes] |
rs7910115 | 1.00[ASN][1000 genomes] |
rs7910864 | 0.88[ASN][1000 genomes] |
rs7911332 | 0.88[ASN][1000 genomes] |
rs7914133 | 0.95[ASN][1000 genomes] |
rs7914794 | 0.95[ASN][1000 genomes] |
rs7915331 | 0.93[ASN][1000 genomes] |
rs7916523 | 0.95[ASN][1000 genomes] |
rs7919797 | 1.00[ASN][1000 genomes] |
rs7920500 | 0.93[ASN][1000 genomes] |
rs7920553 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs7920604 | 0.95[ASN][1000 genomes] |
rs9651433 | 0.85[ASN][1000 genomes] |
rs9804186 | 1.00[ASN][1000 genomes] |
rs9804311 | 0.95[ASN][1000 genomes] |
rs9943307 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1040403 | chr10:93165819-93225036 | Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv895890 | chr10:93176418-93219246 | ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv895891 | chr10:93176418-93269972 | Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS | TF binding regionChromatin interactive regionmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
4 | esv33149 | chr10:93203538-93211658 | ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:93176600-93212600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr10:93184400-93226400 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
3 | chr10:93186000-93226800 | Weak transcription | Pancreas | Pancrea |
4 | chr10:93194600-93213800 | Weak transcription | HUVEC | blood vessel |
5 | chr10:93195600-93213000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr10:93196000-93220600 | Weak transcription | Hela-S3 | cervix |
7 | chr10:93205000-93211800 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
8 | chr10:93205800-93210800 | Weak transcription | Aorta | Aorta |
9 | chr10:93209000-93209600 | ZNF genes & repeats | Cortex derived primary cultured neurospheres | brain |
10 | chr10:93209200-93210000 | ZNF genes & repeats | Fetal Lung | lung |
11 | chr10:93209400-93211800 | Weak transcription | Psoas Muscle | Psoas |