Variant report
Variant | rs28545536 |
---|---|
Chromosome Location | chr2:190260537-190260538 |
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] |
---|---|
rs10153543 | 1.00[ASN][1000 genomes] |
rs10153951 | 1.00[ASN][1000 genomes] |
rs10166669 | 1.00[ASN][1000 genomes] |
rs10166763 | 1.00[ASN][1000 genomes] |
rs10168736 | 1.00[ASN][1000 genomes] |
rs10169952 | 1.00[ASN][1000 genomes] |
rs10170085 | 1.00[ASN][1000 genomes] |
rs10172337 | 1.00[ASN][1000 genomes] |
rs10174122 | 1.00[ASN][1000 genomes] |
rs10174725 | 1.00[ASN][1000 genomes] |
rs10174952 | 1.00[ASN][1000 genomes] |
rs10177339 | 1.00[ASN][1000 genomes] |
rs10177917 | 1.00[ASN][1000 genomes] |
rs10178328 | 1.00[ASN][1000 genomes] |
rs10178743 | 1.00[ASN][1000 genomes] |
rs10179002 | 1.00[ASN][1000 genomes] |
rs10179972 | 1.00[ASN][1000 genomes] |
rs10181872 | 1.00[ASN][1000 genomes] |
rs10182328 | 1.00[ASN][1000 genomes] |
rs10182531 | 1.00[ASN][1000 genomes] |
rs10182637 | 1.00[ASN][1000 genomes] |
rs10184389 | 1.00[ASN][1000 genomes] |
rs10185003 | 1.00[ASN][1000 genomes] |
rs10185694 | 1.00[ASN][1000 genomes] |
rs10186436 | 1.00[ASN][1000 genomes] |
rs10187336 | 1.00[ASN][1000 genomes] |
rs10187808 | 1.00[ASN][1000 genomes] |
rs10187975 | 1.00[ASN][1000 genomes] |
rs10188565 | 1.00[ASN][1000 genomes] |
rs10189469 | 1.00[ASN][1000 genomes] |
rs10190096 | 1.00[ASN][1000 genomes] |
rs10191409 | 1.00[ASN][1000 genomes] |
rs10191847 | 1.00[ASN][1000 genomes] |
rs10193984 | 1.00[ASN][1000 genomes] |
rs10194834 | 1.00[ASN][1000 genomes] |
rs10194934 | 1.00[ASN][1000 genomes] |
rs10196977 | 1.00[ASN][1000 genomes] |
rs10198744 | 1.00[ASN][1000 genomes] |
rs10200629 | 1.00[ASN][1000 genomes] |
rs10201372 | 1.00[ASN][1000 genomes] |
rs10201984 | 1.00[ASN][1000 genomes] |
rs10202436 | 1.00[ASN][1000 genomes] |
rs10202723 | 1.00[ASN][1000 genomes] |
rs10203516 | 1.00[ASN][1000 genomes] |
rs10203719 | 1.00[ASN][1000 genomes] |
rs10204110 | 1.00[ASN][1000 genomes] |
rs10204767 | 1.00[ASN][1000 genomes] |
rs10205215 | 1.00[ASN][1000 genomes] |
rs10205775 | 1.00[ASN][1000 genomes] |
rs10206562 | 1.00[ASN][1000 genomes] |
rs10207004 | 1.00[ASN][1000 genomes] |
rs10207860 | 0.87[EUR][1000 genomes] |
rs10208917 | 1.00[ASN][1000 genomes] |
rs10209758 | 1.00[ASN][1000 genomes] |
rs10221749 | 1.00[ASN][1000 genomes] |
rs10221861 | 1.00[ASN][1000 genomes] |
rs10439311 | 1.00[ASN][1000 genomes] |
rs10439312 | 1.00[ASN][1000 genomes] |
rs10469647 | 1.00[ASN][1000 genomes] |
rs10931412 | 1.00[ASN][1000 genomes] |
rs10931413 | 1.00[ASN][1000 genomes] |
rs12328504 | 1.00[ASN][1000 genomes] |
rs12328515 | 1.00[ASN][1000 genomes] |
rs12328914 | 1.00[ASN][1000 genomes] |
rs13383723 | 1.00[ASN][1000 genomes] |
rs13387876 | 1.00[ASN][1000 genomes] |
rs13387877 | 1.00[ASN][1000 genomes] |
rs13388039 | 1.00[ASN][1000 genomes] |
rs13388779 | 1.00[ASN][1000 genomes] |
rs13391841 | 1.00[ASN][1000 genomes] |
rs13392896 | 1.00[ASN][1000 genomes] |
rs13394718 | 1.00[ASN][1000 genomes] |
rs13396640 | 1.00[ASN][1000 genomes] |
rs13396910 | 1.00[ASN][1000 genomes] |
rs13400624 | 1.00[ASN][1000 genomes] |
rs13402678 | 1.00[ASN][1000 genomes] |
rs13402923 | 1.00[ASN][1000 genomes] |
rs13405433 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13407353 | 1.00[ASN][1000 genomes] |
rs13407452 | 1.00[ASN][1000 genomes] |
rs13407566 | 1.00[ASN][1000 genomes] |
rs13409397 | 1.00[ASN][1000 genomes] |
rs13413979 | 1.00[ASN][1000 genomes] |
rs13414763 | 1.00[ASN][1000 genomes] |
rs13418443 | 1.00[ASN][1000 genomes] |
rs13419269 | 1.00[ASN][1000 genomes] |
rs13419984 | 1.00[ASN][1000 genomes] |
rs13420832 | 1.00[ASN][1000 genomes] |
rs13423429 | 1.00[ASN][1000 genomes] |
rs13423654 | 1.00[ASN][1000 genomes] |
rs13424586 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13425539 | 1.00[ASN][1000 genomes] |
rs13425989 | 1.00[ASN][1000 genomes] |
rs13426851 | 1.00[ASN][1000 genomes] |
rs13427092 | 1.00[ASN][1000 genomes] |
rs13427686 | 1.00[ASN][1000 genomes] |
rs13432036 | 1.00[ASN][1000 genomes] |
rs13432963 | 1.00[ASN][1000 genomes] |
rs28368169 | 1.00[ASN][1000 genomes] |
rs28414300 | 1.00[ASN][1000 genomes] |
rs28433254 | 1.00[ASN][1000 genomes] |
rs28567040 | 1.00[ASN][1000 genomes] |
rs28679474 | 1.00[ASN][1000 genomes] |
rs55808493 | 1.00[ASN][1000 genomes] |
rs55819631 | 1.00[ASN][1000 genomes] |
rs56996340 | 1.00[ASN][1000 genomes] |
rs57215654 | 1.00[ASN][1000 genomes] |
rs57398906 | 1.00[ASN][1000 genomes] |
rs57458325 | 1.00[ASN][1000 genomes] |
rs57598703 | 1.00[ASN][1000 genomes] |
rs58396131 | 1.00[ASN][1000 genomes] |
rs59506401 | 1.00[ASN][1000 genomes] |
rs59826931 | 1.00[ASN][1000 genomes] |
rs59872509 | 1.00[ASN][1000 genomes] |
rs60056080 | 1.00[ASN][1000 genomes] |
rs60708586 | 1.00[ASN][1000 genomes] |
rs61154892 | 1.00[ASN][1000 genomes] |
rs61625679 | 1.00[ASN][1000 genomes] |
rs6414123 | 0.87[EUR][1000 genomes] |
rs6717036 | 1.00[ASN][1000 genomes] |
rs6724634 | 1.00[ASN][1000 genomes] |
rs6746050 | 1.00[ASN][1000 genomes] |
rs6761847 | 0.87[EUR][1000 genomes] |
rs7355598 | 1.00[ASN][1000 genomes] |
rs73978605 | 1.00[ASN][1000 genomes] |
rs73980173 | 1.00[ASN][1000 genomes] |
rs73980174 | 1.00[ASN][1000 genomes] |
rs73980175 | 1.00[ASN][1000 genomes] |
rs73980177 | 1.00[ASN][1000 genomes] |
rs73980180 | 1.00[ASN][1000 genomes] |
rs73980182 | 1.00[ASN][1000 genomes] |
rs73980183 | 1.00[ASN][1000 genomes] |
rs73980187 | 1.00[ASN][1000 genomes] |
rs73980188 | 1.00[ASN][1000 genomes] |
rs73980190 | 1.00[ASN][1000 genomes] |
rs73980191 | 1.00[ASN][1000 genomes] |
rs73980192 | 1.00[ASN][1000 genomes] |
rs73980193 | 1.00[ASN][1000 genomes] |
rs73980194 | 1.00[ASN][1000 genomes] |
rs73980195 | 1.00[ASN][1000 genomes] |
rs73980196 | 1.00[ASN][1000 genomes] |
rs73980197 | 1.00[ASN][1000 genomes] |
rs73980198 | 1.00[ASN][1000 genomes] |
rs73980199 | 1.00[ASN][1000 genomes] |
rs73980201 | 1.00[ASN][1000 genomes] |
rs73980202 | 1.00[ASN][1000 genomes] |
rs73982004 | 1.00[ASN][1000 genomes] |
rs73982007 | 1.00[ASN][1000 genomes] |
rs73982032 | 1.00[ASN][1000 genomes] |
rs73982033 | 1.00[ASN][1000 genomes] |
rs73982034 | 1.00[ASN][1000 genomes] |
rs73982037 | 1.00[ASN][1000 genomes] |
rs7558500 | 1.00[ASN][1000 genomes] |
rs7561643 | 1.00[ASN][1000 genomes] |
rs7562592 | 1.00[ASN][1000 genomes] |
rs7566271 | 1.00[ASN][1000 genomes] |
rs7569974 | 1.00[ASN][1000 genomes] |
rs7582435 | 0.87[EUR][1000 genomes] |
rs7584984 | 1.00[ASN][1000 genomes] |
rs7599216 | 0.87[EUR][1000 genomes] |
rs7599676 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7606355 | 0.87[EUR][1000 genomes] |
rs7609327 | 1.00[ASN][1000 genomes] |
rs9288164 | 1.00[ASN][1000 genomes] |
rs9808058 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533029 | chr2:189812229-190554339 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
2 | nsv875613 | chr2:189999011-190324685 | Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
3 | nsv875615 | chr2:190215527-190444392 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
4 | esv3451292 | chr2:190225623-190266276 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:190253400-190268000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
2 | chr2:190258800-190264400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr2:190258800-190272000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr2:190258800-190272600 | Weak transcription | Aorta | Aorta |
5 | chr2:190260400-190260600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |