Variant report
Variant | rs62097103 |
---|---|
Chromosome Location | chr18:12576367-12576368 |
allele | C/G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:3 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10401097 | 0.84[ASN][1000 genomes] |
rs10445428 | 0.94[ASN][1000 genomes] |
rs11080582 | 0.94[ASN][1000 genomes] |
rs11080583 | 0.92[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs11080584 | 0.95[ASN][1000 genomes] |
rs11080585 | 0.86[ASN][1000 genomes] |
rs11080586 | 0.86[ASN][1000 genomes] |
rs11080590 | 0.84[ASN][1000 genomes] |
rs11659854 | 0.86[ASN][1000 genomes] |
rs11663958 | 0.87[ASN][1000 genomes] |
rs11664404 | 0.82[ASN][1000 genomes] |
rs11664765 | 0.84[ASN][1000 genomes] |
rs11664861 | 0.88[ASN][1000 genomes] |
rs11664914 | 0.88[ASN][1000 genomes] |
rs11664917 | 0.88[ASN][1000 genomes] |
rs11664927 | 0.82[ASN][1000 genomes] |
rs11664936 | 0.86[ASN][1000 genomes] |
rs11665543 | 0.86[ASN][1000 genomes] |
rs12326271 | 0.85[ASN][1000 genomes] |
rs12454931 | 0.85[ASN][1000 genomes] |
rs12455093 | 0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs12455536 | 0.84[ASN][1000 genomes] |
rs12455892 | 0.80[ASN][1000 genomes] |
rs12455909 | 0.88[ASN][1000 genomes] |
rs12457903 | 0.90[AFR][1000 genomes];0.92[ASN][1000 genomes] |
rs12604184 | 0.84[ASN][1000 genomes] |
rs12604385 | 0.90[ASN][1000 genomes] |
rs12604400 | 0.83[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs12604541 | 0.85[ASN][1000 genomes] |
rs12605240 | 0.89[ASN][1000 genomes] |
rs12605392 | 0.88[ASN][1000 genomes] |
rs12606506 | 0.81[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs12709540 | 0.86[ASN][1000 genomes] |
rs12953406 | 0.94[ASN][1000 genomes] |
rs12953578 | 0.84[ASN][1000 genomes] |
rs12954614 | 0.98[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs12955161 | 0.90[ASN][1000 genomes] |
rs12955490 | 0.89[ASN][1000 genomes] |
rs12956133 | 0.84[ASN][1000 genomes] |
rs12956385 | 0.83[ASN][1000 genomes] |
rs12956885 | 0.88[ASN][1000 genomes] |
rs12957048 | 0.82[ASN][1000 genomes] |
rs12957151 | 0.95[ASN][1000 genomes] |
rs12957688 | 0.89[ASN][1000 genomes] |
rs12958200 | 0.85[ASN][1000 genomes] |
rs12959015 | 0.81[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs12960150 | 0.84[ASN][1000 genomes] |
rs12961695 | 0.84[ASN][1000 genomes] |
rs12961966 | 0.94[ASN][1000 genomes] |
rs12962476 | 0.88[ASN][1000 genomes] |
rs12963179 | 0.89[ASN][1000 genomes] |
rs12963325 | 0.90[ASN][1000 genomes] |
rs12964660 | 0.92[ASN][1000 genomes] |
rs12965094 | 0.81[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs12970025 | 0.86[ASN][1000 genomes] |
rs12970174 | 0.86[AMR][1000 genomes];0.99[ASN][1000 genomes] |
rs1893193 | 0.92[ASN][1000 genomes] |
rs1940974 | 0.89[ASN][1000 genomes] |
rs1940975 | 0.86[ASN][1000 genomes] |
rs2155698 | 0.86[ASN][1000 genomes] |
rs2186907 | 0.86[ASN][1000 genomes] |
rs28414067 | 0.85[ASN][1000 genomes] |
rs28457089 | 0.81[ASN][1000 genomes] |
rs28496036 | 0.90[ASN][1000 genomes] |
rs28582228 | 0.86[ASN][1000 genomes] |
rs28886423 | 0.88[ASN][1000 genomes] |
rs34072260 | 0.81[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs34178879 | 0.94[ASN][1000 genomes] |
rs34438212 | 0.83[AFR][1000 genomes] |
rs34456643 | 0.94[ASN][1000 genomes] |
rs34814556 | 0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs34899007 | 0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs35122110 | 0.88[ASN][1000 genomes] |
rs35449211 | 0.86[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs35630805 | 0.87[ASN][1000 genomes] |
rs35963756 | 0.92[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs4389196 | 0.88[ASN][1000 genomes] |
rs4493131 | 0.81[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs4627434 | 0.86[ASN][1000 genomes] |
rs4629035 | 0.84[ASN][1000 genomes] |
rs55749182 | 0.92[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs58215411 | 0.93[ASN][1000 genomes] |
rs60505421 | 0.88[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs62097094 | 0.83[ASN][1000 genomes] |
rs62097102 | 0.86[AMR][1000 genomes];0.99[ASN][1000 genomes] |
rs62097126 | 0.89[ASN][1000 genomes] |
rs62097148 | 0.87[ASN][1000 genomes] |
rs62097149 | 0.84[ASN][1000 genomes] |
rs62097152 | 0.83[ASN][1000 genomes] |
rs62097153 | 0.85[ASN][1000 genomes] |
rs67045810 | 0.85[ASN][1000 genomes] |
rs67268432 | 0.92[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs722708 | 0.84[ASN][1000 genomes] |
rs7234697 | 0.89[ASN][1000 genomes] |
rs7237732 | 0.81[ASN][1000 genomes] |
rs7238080 | 0.82[ASN][1000 genomes] |
rs723836 | 0.85[ASN][1000 genomes] |
rs7238546 | 0.85[ASN][1000 genomes] |
rs7242395 | 0.83[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs7504857 | 0.83[ASN][1000 genomes] |
rs755020 | 0.88[ASN][1000 genomes] |
rs755021 | 0.88[ASN][1000 genomes] |
rs8086094 | 0.88[ASN][1000 genomes] |
rs8087885 | 0.88[ASN][1000 genomes] |
rs8088786 | 0.85[ASN][1000 genomes] |
rs8089081 | 0.90[ASN][1000 genomes] |
rs8089115 | 0.82[ASN][1000 genomes] |
rs8089619 | 0.92[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs8093129 | 0.88[ASN][1000 genomes] |
rs8093571 | 0.81[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs8095160 | 0.86[ASN][1000 genomes] |
rs8096455 | 0.84[ASN][1000 genomes] |
rs9303772 | 0.84[ASN][1000 genomes] |
rs9303773 | 0.84[ASN][1000 genomes] |
rs948301 | 0.88[ASN][1000 genomes] |
rs948302 | 0.88[ASN][1000 genomes] |
rs9675543 | 0.88[ASN][1000 genomes] |
rs9945339 | 0.85[ASN][1000 genomes] |
rs9947738 | 0.87[ASN][1000 genomes] |
rs9948505 | 0.84[ASN][1000 genomes] |
rs9948618 | 0.83[ASN][1000 genomes] |
rs9951147 | 0.89[ASN][1000 genomes] |
rs9954054 | 0.84[ASN][1000 genomes] |
rs9958409 | 0.84[ASN][1000 genomes] |
rs9959759 | 0.89[ASN][1000 genomes] |
rs9960824 | 0.83[ASN][1000 genomes] |
rs9961851 | 0.85[ASN][1000 genomes] |
rs9964759 | 0.87[ASN][1000 genomes] |
rs9965123 | 0.84[ASN][1000 genomes] |
rs9989496 | 0.84[ASN][1000 genomes] |
rs9989506 | 0.84[ASN][1000 genomes] |
rs9989568 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1063125 | chr18:12046892-12918251 | Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 130 gene(s) | inside rSNPs | diseases |
2 | nsv491873 | chr18:12159445-12739784 | Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 79 gene(s) | inside rSNPs | diseases |
3 | nsv909400 | chr18:12201374-12585545 | Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
4 | esv3528039 | chr18:12396582-12851293 | Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 36 gene(s) | inside rSNPs | diseases |
5 | esv3528041 | chr18:12396641-12851245 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 36 gene(s) | inside rSNPs | diseases |
6 | nsv523743 | chr18:12474505-12742809 | Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:12557600-12580800 | Weak transcription | Pancreas | Pancrea |
2 | chr18:12570000-12595600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr18:12570200-12578400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
4 | chr18:12570200-12581800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr18:12576000-12581200 | Weak transcription | HepG2 | liver |