Variant report
Variant | rs13016181 |
---|---|
Chromosome Location | chr2:187240962-187240963 |
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] |
---|---|
rs10172511 | 0.86[ASN][1000 genomes] |
rs10188807 | 0.83[ASN][1000 genomes] |
rs10189971 | 0.87[ASN][1000 genomes] |
rs10193268 | 0.86[ASN][1000 genomes] |
rs10194541 | 0.85[ASN][1000 genomes] |
rs10194719 | 0.86[ASN][1000 genomes] |
rs10196208 | 0.84[ASN][1000 genomes] |
rs10203879 | 0.86[ASN][1000 genomes] |
rs10205506 | 0.87[ASN][1000 genomes] |
rs10205705 | 0.87[ASN][1000 genomes] |
rs10210844 | 0.80[ASN][1000 genomes] |
rs1026118 | 0.86[ASN][1000 genomes] |
rs10439308 | 0.83[ASN][1000 genomes] |
rs10804003 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10804004 | 0.99[ASN][1000 genomes] |
rs10931239 | 0.86[ASN][1000 genomes] |
rs10931242 | 0.86[ASN][1000 genomes] |
rs11676936 | 0.87[ASN][1000 genomes] |
rs11683595 | 0.86[ASN][1000 genomes] |
rs11693737 | 0.84[ASN][1000 genomes] |
rs11884786 | 0.83[ASN][1000 genomes] |
rs11889909 | 0.87[ASN][1000 genomes] |
rs12052331 | 0.83[ASN][1000 genomes] |
rs12463831 | 0.83[ASN][1000 genomes] |
rs12464846 | 0.83[ASN][1000 genomes] |
rs12467212 | 0.85[ASN][1000 genomes] |
rs12467891 | 0.99[ASN][1000 genomes] |
rs12469301 | 0.95[ASN][1000 genomes] |
rs12470370 | 0.90[ASN][1000 genomes] |
rs12473076 | 0.82[ASN][1000 genomes] |
rs12473542 | 0.86[ASN][1000 genomes] |
rs12475522 | 0.84[ASN][1000 genomes] |
rs12476313 | 0.82[ASN][1000 genomes] |
rs12477683 | 0.85[ASN][1000 genomes] |
rs12478370 | 0.98[ASN][1000 genomes] |
rs12611673 | 0.82[ASN][1000 genomes] |
rs12612249 | 0.83[ASN][1000 genomes] |
rs12614800 | 0.91[ASN][1000 genomes] |
rs12615503 | 0.83[ASN][1000 genomes] |
rs12615675 | 0.94[ASN][1000 genomes] |
rs12619990 | 0.83[ASN][1000 genomes] |
rs12620626 | 0.83[ASN][1000 genomes] |
rs12623611 | 0.99[ASN][1000 genomes] |
rs12693444 | 0.84[ASN][1000 genomes] |
rs12693447 | 0.85[ASN][1000 genomes] |
rs12693448 | 0.87[ASN][1000 genomes] |
rs12693449 | 0.86[ASN][1000 genomes] |
rs12993773 | 0.85[ASN][1000 genomes] |
rs12998229 | 0.86[ASN][1000 genomes] |
rs12999247 | 0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12999438 | 0.83[ASN][1000 genomes] |
rs13003337 | 0.86[ASN][1000 genomes] |
rs13009502 | 0.88[ASN][1000 genomes] |
rs13011581 | 0.83[ASN][1000 genomes] |
rs13015996 | 0.99[ASN][1000 genomes] |
rs13016273 | 0.90[ASN][1000 genomes] |
rs13017038 | 0.81[ASN][1000 genomes] |
rs13018467 | 0.99[ASN][1000 genomes] |
rs13023992 | 0.95[ASN][1000 genomes] |
rs13024310 | 0.96[ASN][1000 genomes] |
rs13025505 | 0.82[ASN][1000 genomes] |
rs13027135 | 0.86[ASN][1000 genomes] |
rs13029473 | 0.98[ASN][1000 genomes] |
rs13029766 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs13029818 | 0.83[ASN][1000 genomes] |
rs13029980 | 0.95[ASN][1000 genomes] |
rs13030324 | 0.86[ASN][1000 genomes] |
rs13409734 | 0.84[ASN][1000 genomes] |
rs13421394 | 0.95[ASN][1000 genomes] |
rs13421948 | 0.84[ASN][1000 genomes] |
rs13426333 | 0.82[ASN][1000 genomes] |
rs1349154 | 0.87[ASN][1000 genomes] |
rs1375321 | 0.87[ASN][1000 genomes] |
rs1375324 | 0.86[ASN][1000 genomes] |
rs1375325 | 0.86[ASN][1000 genomes] |
rs1375327 | 0.86[ASN][1000 genomes] |
rs1375328 | 0.86[ASN][1000 genomes] |
rs1448851 | 0.87[ASN][1000 genomes] |
rs1448852 | 0.87[ASN][1000 genomes] |
rs1448854 | 0.87[ASN][1000 genomes] |
rs1448856 | 0.99[ASN][1000 genomes] |
rs1448858 | 0.99[ASN][1000 genomes] |
rs1448860 | 0.87[ASN][1000 genomes] |
rs1448861 | 0.86[ASN][1000 genomes] |
rs1448863 | 0.80[ASN][1000 genomes] |
rs1451874 | 0.82[ASN][1000 genomes] |
rs1562646 | 0.86[ASN][1000 genomes] |
rs1562647 | 0.86[ASN][1000 genomes] |
rs1900835 | 0.82[ASN][1000 genomes] |
rs1992930 | 0.83[ASN][1000 genomes] |
rs2084485 | 0.86[ASN][1000 genomes] |
rs2084486 | 0.82[ASN][1000 genomes] |
rs2122087 | 0.83[ASN][1000 genomes] |
rs2197816 | 0.87[ASN][1000 genomes] |
rs2370667 | 0.82[ASN][1000 genomes] |
rs2370691 | 0.87[ASN][1000 genomes] |
rs2370692 | 0.86[ASN][1000 genomes] |
rs28498768 | 0.84[ASN][1000 genomes] |
rs2887819 | 0.82[ASN][1000 genomes] |
rs3107167 | 0.84[ASN][1000 genomes] |
rs3107177 | 0.81[ASN][1000 genomes] |
rs3107406 | 0.83[ASN][1000 genomes] |
rs3107414 | 0.84[ASN][1000 genomes] |
rs3112322 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4130801 | 0.82[ASN][1000 genomes] |
rs4144824 | 0.83[ASN][1000 genomes] |
rs4271735 | 0.96[ASN][1000 genomes] |
rs4341896 | 0.99[ASN][1000 genomes] |
rs4363995 | 0.92[ASN][1000 genomes] |
rs4430906 | 0.95[ASN][1000 genomes] |
rs4522568 | 0.82[ASN][1000 genomes] |
rs4530331 | 0.84[ASN][1000 genomes] |
rs4569437 | 0.95[ASN][1000 genomes] |
rs4608482 | 0.89[ASN][1000 genomes] |
rs4637073 | 0.81[ASN][1000 genomes] |
rs4666701 | 0.86[ASN][1000 genomes] |
rs4666703 | 0.86[ASN][1000 genomes] |
rs4667079 | 0.83[ASN][1000 genomes] |
rs4667080 | 0.83[ASN][1000 genomes] |
rs4667081 | 0.85[ASN][1000 genomes] |
rs4667086 | 0.86[ASN][1000 genomes] |
rs4667089 | 0.83[ASN][1000 genomes] |
rs4667090 | 0.94[ASN][1000 genomes] |
rs4667092 | 0.86[ASN][1000 genomes] |
rs4667095 | 0.84[ASN][1000 genomes] |
rs5008098 | 0.82[ASN][1000 genomes] |
rs56347348 | 0.98[ASN][1000 genomes] |
rs56393956 | 0.83[ASN][1000 genomes] |
rs56681734 | 0.84[ASN][1000 genomes] |
rs56718299 | 0.83[ASN][1000 genomes] |
rs56786415 | 0.82[ASN][1000 genomes] |
rs57289110 | 0.83[ASN][1000 genomes] |
rs58244659 | 0.83[ASN][1000 genomes] |
rs58488407 | 0.82[ASN][1000 genomes] |
rs58579412 | 0.83[ASN][1000 genomes] |
rs58783284 | 0.84[ASN][1000 genomes] |
rs59087873 | 0.82[ASN][1000 genomes] |
rs59224241 | 0.83[ASN][1000 genomes] |
rs59276018 | 0.84[ASN][1000 genomes] |
rs59360834 | 0.82[ASN][1000 genomes] |
rs60859807 | 0.83[ASN][1000 genomes] |
rs61083860 | 0.83[ASN][1000 genomes] |
rs61253791 | 0.83[ASN][1000 genomes] |
rs6434170 | 0.86[ASN][1000 genomes] |
rs6434171 | 0.87[ASN][1000 genomes] |
rs6434179 | 0.83[ASN][1000 genomes] |
rs6434182 | 0.83[ASN][1000 genomes] |
rs6434183 | 0.83[ASN][1000 genomes] |
rs66593320 | 0.83[ASN][1000 genomes] |
rs6704957 | 0.98[ASN][1000 genomes] |
rs6712627 | 0.86[ASN][1000 genomes] |
rs6715735 | 0.95[ASN][1000 genomes] |
rs6717965 | 0.86[ASN][1000 genomes] |
rs6728734 | 0.86[ASN][1000 genomes] |
rs6741525 | 0.83[ASN][1000 genomes] |
rs6742943 | 0.87[ASN][1000 genomes] |
rs6743356 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6744814 | 0.84[ASN][1000 genomes] |
rs6745187 | 0.83[ASN][1000 genomes] |
rs6745873 | 0.86[ASN][1000 genomes] |
rs6752407 | 0.80[ASN][1000 genomes] |
rs6754898 | 0.83[ASN][1000 genomes] |
rs6755955 | 0.86[ASN][1000 genomes] |
rs6759502 | 0.80[ASN][1000 genomes] |
rs6760230 | 0.83[ASN][1000 genomes] |
rs67917059 | 0.82[ASN][1000 genomes] |
rs716130 | 0.85[ASN][1000 genomes] |
rs72907565 | 0.83[ASN][1000 genomes] |
rs73035230 | 0.82[ASN][1000 genomes] |
rs73035235 | 0.83[ASN][1000 genomes] |
rs73035261 | 0.83[ASN][1000 genomes] |
rs7558599 | 0.86[ASN][1000 genomes] |
rs7560019 | 0.84[ASN][1000 genomes] |
rs7571191 | 0.83[ASN][1000 genomes] |
rs7571408 | 0.84[ASN][1000 genomes] |
rs7573296 | 0.89[ASN][1000 genomes] |
rs7579391 | 0.94[ASN][1000 genomes] |
rs7580038 | 0.99[ASN][1000 genomes] |
rs7581081 | 0.81[ASN][1000 genomes] |
rs7586276 | 0.81[ASN][1000 genomes] |
rs7586291 | 0.80[ASN][1000 genomes] |
rs7587077 | 0.81[ASN][1000 genomes] |
rs7587079 | 0.82[ASN][1000 genomes] |
rs7597285 | 0.82[ASN][1000 genomes] |
rs7602918 | 0.86[ASN][1000 genomes] |
rs7606494 | 0.87[ASN][1000 genomes] |
rs980540 | 0.87[ASN][1000 genomes] |
rs9807987 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv875545 | chr2:186566024-187280164 | Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv868949 | chr2:186657142-187327560 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
3 | nsv932296 | chr2:186737443-187265790 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
4 | nsv1006411 | chr2:187150025-187291081 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv536079 | chr2:187150025-187291081 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv428067 | chr2:187171324-187334779 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv961744 | chr2:187189976-187265519 | Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
8 | nsv3071 | chr2:187208040-187252682 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv963887 | chr2:187239111-187253365 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:187240000-187243600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr2:187240600-187241200 | ZNF genes & repeats | Fetal Intestine Small | intestine |
3 | chr2:187240600-187241400 | Enhancers | Placenta | Placenta |