Variant report
Variant | rs4398852 |
---|---|
Chromosome Location | chr7:48588706-48588707 |
allele | A/T |
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] |
---|---|
rs10499684 | 0.87[ASN][1000 genomes] |
rs11185608 | 0.87[ASN][1000 genomes] |
rs11185609 | 0.87[ASN][1000 genomes] |
rs12112361 | 0.95[ASN][1000 genomes] |
rs12113920 | 0.95[ASN][1000 genomes] |
rs12113960 | 0.95[ASN][1000 genomes] |
rs12667982 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12669930 | 0.80[ASN][1000 genomes] |
rs12669976 | 0.80[ASN][1000 genomes] |
rs12670340 | 0.95[ASN][1000 genomes] |
rs12671073 | 0.95[ASN][1000 genomes] |
rs12672551 | 0.95[ASN][1000 genomes] |
rs12673070 | 0.83[ASN][1000 genomes] |
rs12674401 | 0.94[ASN][1000 genomes] |
rs12674424 | 0.92[ASN][1000 genomes] |
rs1316349 | 0.95[ASN][1000 genomes] |
rs1317162 | 0.94[ASN][1000 genomes] |
rs13237819 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1527835 | 0.93[ASN][1000 genomes] |
rs1527839 | 0.91[ASN][1000 genomes] |
rs1609212 | 0.95[ASN][1000 genomes] |
rs1609213 | 0.95[ASN][1000 genomes] |
rs1609214 | 0.95[ASN][1000 genomes] |
rs17092931 | 0.95[ASN][1000 genomes] |
rs17132425 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs17132430 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs17132439 | 0.95[ASN][1000 genomes] |
rs17132443 | 0.95[ASN][1000 genomes] |
rs17132460 | 0.95[ASN][1000 genomes] |
rs17132479 | 0.95[ASN][1000 genomes] |
rs17132491 | 0.95[ASN][1000 genomes] |
rs1918580 | 0.95[ASN][1000 genomes] |
rs1918581 | 0.95[ASN][1000 genomes] |
rs1918586 | 0.95[ASN][1000 genomes] |
rs1918587 | 0.95[ASN][1000 genomes] |
rs1918588 | 0.95[ASN][1000 genomes] |
rs1918589 | 0.95[ASN][1000 genomes] |
rs1918594 | 0.85[ASN][1000 genomes] |
rs1918595 | 0.94[ASN][1000 genomes] |
rs1918596 | 0.95[ASN][1000 genomes] |
rs1918597 | 0.95[ASN][1000 genomes] |
rs1918598 | 0.95[ASN][1000 genomes] |
rs1918600 | 0.92[ASN][1000 genomes] |
rs1918601 | 0.95[ASN][1000 genomes] |
rs1918602 | 0.95[ASN][1000 genomes] |
rs1918606 | 0.92[ASN][1000 genomes] |
rs1918608 | 0.95[ASN][1000 genomes] |
rs2141251 | 0.95[ASN][1000 genomes] |
rs2178086 | 0.95[ASN][1000 genomes] |
rs2178087 | 0.95[ASN][1000 genomes] |
rs2222731 | 0.95[ASN][1000 genomes] |
rs34252471 | 0.95[ASN][1000 genomes] |
rs4072501 | 0.95[ASN][1000 genomes] |
rs4072502 | 0.95[ASN][1000 genomes] |
rs4072503 | 0.95[ASN][1000 genomes] |
rs41332948 | 0.95[ASN][1000 genomes] |
rs4144061 | 0.92[ASN][1000 genomes] |
rs4144063 | 0.95[ASN][1000 genomes] |
rs4144064 | 0.95[ASN][1000 genomes] |
rs4144067 | 0.95[ASN][1000 genomes] |
rs4144068 | 0.92[ASN][1000 genomes] |
rs4295610 | 0.95[ASN][1000 genomes] |
rs4296993 | 0.95[ASN][1000 genomes] |
rs4587280 | 0.95[ASN][1000 genomes] |
rs55735040 | 0.87[ASN][1000 genomes] |
rs55903755 | 0.94[ASN][1000 genomes] |
rs55974693 | 0.87[ASN][1000 genomes] |
rs56134922 | 0.92[ASN][1000 genomes] |
rs56205257 | 0.95[ASN][1000 genomes] |
rs56213942 | 0.94[ASN][1000 genomes] |
rs56241442 | 0.95[ASN][1000 genomes] |
rs56393952 | 0.95[ASN][1000 genomes] |
rs56408667 | 0.87[ASN][1000 genomes] |
rs56798342 | 0.95[ASN][1000 genomes] |
rs56806901 | 0.95[ASN][1000 genomes] |
rs57226042 | 0.86[ASN][1000 genomes] |
rs57370511 | 0.86[ASN][1000 genomes] |
rs57401097 | 0.95[ASN][1000 genomes] |
rs57877708 | 0.95[ASN][1000 genomes] |
rs58077564 | 0.95[ASN][1000 genomes] |
rs58321909 | 0.93[ASN][1000 genomes] |
rs58433353 | 0.95[ASN][1000 genomes] |
rs58481134 | 0.87[ASN][1000 genomes] |
rs58486673 | 0.95[ASN][1000 genomes] |
rs58635193 | 0.95[ASN][1000 genomes] |
rs59100514 | 0.95[ASN][1000 genomes] |
rs59227959 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs59243715 | 0.95[ASN][1000 genomes] |
rs59549039 | 0.95[ASN][1000 genomes] |
rs59673264 | 0.95[ASN][1000 genomes] |
rs59872216 | 0.82[ASN][1000 genomes] |
rs60184691 | 0.95[ASN][1000 genomes] |
rs60813775 | 0.85[ASN][1000 genomes] |
rs60918397 | 0.95[ASN][1000 genomes] |
rs61171557 | 0.95[ASN][1000 genomes] |
rs61310674 | 0.95[ASN][1000 genomes] |
rs61602397 | 0.95[ASN][1000 genomes] |
rs61649354 | 0.95[ASN][1000 genomes] |
rs61706229 | 0.87[ASN][1000 genomes] |
rs6583452 | 0.95[ASN][1000 genomes] |
rs6583456 | 0.98[ASN][1000 genomes] |
rs66522605 | 0.95[ASN][1000 genomes] |
rs66591834 | 0.95[ASN][1000 genomes] |
rs66729625 | 0.95[ASN][1000 genomes] |
rs66763020 | 0.95[ASN][1000 genomes] |
rs66785002 | 0.95[ASN][1000 genomes] |
rs66793444 | 0.95[ASN][1000 genomes] |
rs66909576 | 0.95[ASN][1000 genomes] |
rs67001204 | 0.80[ASN][1000 genomes] |
rs67040412 | 0.93[ASN][1000 genomes] |
rs67074321 | 0.95[ASN][1000 genomes] |
rs67081192 | 0.95[ASN][1000 genomes] |
rs67187623 | 0.95[ASN][1000 genomes] |
rs67208890 | 0.94[ASN][1000 genomes] |
rs67249167 | 0.95[ASN][1000 genomes] |
rs67249859 | 0.95[ASN][1000 genomes] |
rs67294077 | 0.87[ASN][1000 genomes] |
rs67298249 | 0.95[ASN][1000 genomes] |
rs67316911 | 0.94[ASN][1000 genomes] |
rs67331245 | 0.95[ASN][1000 genomes] |
rs67370671 | 0.95[ASN][1000 genomes] |
rs67398358 | 0.95[ASN][1000 genomes] |
rs67744396 | 0.95[ASN][1000 genomes] |
rs67744565 | 0.95[ASN][1000 genomes] |
rs67748204 | 0.95[ASN][1000 genomes] |
rs67764854 | 0.95[ASN][1000 genomes] |
rs67845756 | 0.95[ASN][1000 genomes] |
rs67852079 | 0.95[ASN][1000 genomes] |
rs67875048 | 0.87[ASN][1000 genomes] |
rs68007434 | 0.95[ASN][1000 genomes] |
rs68029531 | 0.95[ASN][1000 genomes] |
rs68084496 | 0.95[ASN][1000 genomes] |
rs68110103 | 0.95[ASN][1000 genomes] |
rs68168969 | 0.95[ASN][1000 genomes] |
rs68179951 | 0.95[ASN][1000 genomes] |
rs6944801 | 0.95[ASN][1000 genomes] |
rs6954223 | 0.93[ASN][1000 genomes] |
rs6955102 | 0.95[ASN][1000 genomes] |
rs6957309 | 0.95[ASN][1000 genomes] |
rs6963717 | 0.95[ASN][1000 genomes] |
rs6966994 | 0.95[ASN][1000 genomes] |
rs6970434 | 0.93[ASN][1000 genomes] |
rs6972202 | 0.95[ASN][1000 genomes] |
rs6977997 | 0.95[ASN][1000 genomes] |
rs6980042 | 0.95[ASN][1000 genomes] |
rs6980069 | 0.95[ASN][1000 genomes] |
rs73094625 | 0.95[ASN][1000 genomes] |
rs73109344 | 0.95[ASN][1000 genomes] |
rs73109355 | 0.95[ASN][1000 genomes] |
rs73109362 | 0.94[ASN][1000 genomes] |
rs73109364 | 0.95[ASN][1000 genomes] |
rs73109382 | 0.94[ASN][1000 genomes] |
rs73109385 | 0.94[ASN][1000 genomes] |
rs73109399 | 0.94[ASN][1000 genomes] |
rs73109401 | 0.95[ASN][1000 genomes] |
rs73111405 | 0.95[ASN][1000 genomes] |
rs7455877 | 0.95[ASN][1000 genomes] |
rs7457791 | 0.95[ASN][1000 genomes] |
rs7776966 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7778895 | 0.94[ASN][1000 genomes] |
rs7781149 | 0.95[ASN][1000 genomes] |
rs7785069 | 0.95[ASN][1000 genomes] |
rs7791044 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7792728 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7797852 | 0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7804139 | 0.95[ASN][1000 genomes] |
rs7806480 | 0.95[ASN][1000 genomes] |
rs7807529 | 0.95[ASN][1000 genomes] |
rs7810275 | 0.94[ASN][1000 genomes] |
rs9690617 | 0.95[ASN][1000 genomes] |
rs9691143 | 0.95[ASN][1000 genomes] |
rs9691391 | 0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830992 | chr7:48497408-48686442 | Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
2 | nsv888008 | chr7:48568425-48652224 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | n/a | n/a | inside rSNPs | diseases |
3 | esv2764056 | chr7:48580914-48592025 | Enhancers Strong transcription Weak transcription | n/a | n/a | inside rSNPs | diseases |
4 | esv11768 | chr7:48581423-48592171 | Weak transcription Enhancers Strong transcription | n/a | n/a | inside rSNPs | diseases |
5 | nsv514416 | chr7:48581830-48592050 | Enhancers Weak transcription Strong transcription | n/a | n/a | inside rSNPs | diseases |
6 | esv1818564 | chr7:48581852-48592025 | Strong transcription Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
7 | esv2421774 | chr7:48581852-48592025 | Enhancers Weak transcription Strong transcription | n/a | n/a | inside rSNPs | diseases |
8 | nsv442042 | chr7:48581852-48592025 | Weak transcription Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
9 | nsv527625 | chr7:48586783-48596337 | Enhancers Weak transcription Strong transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:48588000-48589200 | Strong transcription | Primary neutrophils fromperipheralblood | blood |
2 | chr7:48588200-48588800 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
3 | chr7:48588600-48588800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |