Variant report
Variant | rs10934138 |
---|---|
Chromosome Location | chr3:111938647-111938648 |
allele | C/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] |
---|---|
rs10511309 | 0.87[ASN][1000 genomes] |
rs10934158 | 0.83[EUR][1000 genomes] |
rs1119338 | 0.83[EUR][1000 genomes] |
rs11712289 | 0.83[EUR][1000 genomes] |
rs11714145 | 0.83[EUR][1000 genomes] |
rs11714273 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11928353 | 0.90[ASN][1000 genomes] |
rs12054138 | 0.81[ASN][1000 genomes] |
rs12493824 | 0.87[ASN][1000 genomes] |
rs12494678 | 0.83[EUR][1000 genomes] |
rs12629465 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12632408 | 0.81[EUR][1000 genomes] |
rs12634031 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12638964 | 0.83[EUR][1000 genomes] |
rs13060187 | 0.87[ASN][1000 genomes] |
rs13064510 | 0.87[ASN][1000 genomes] |
rs13067030 | 0.89[ASN][1000 genomes] |
rs13069887 | 0.87[ASN][1000 genomes] |
rs13079745 | 0.87[ASN][1000 genomes] |
rs13088733 | 0.81[ASN][1000 genomes] |
rs13314792 | 0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs13314977 | 0.81[EUR][1000 genomes] |
rs13315900 | 0.86[ASN][1000 genomes] |
rs13327160 | 0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13327165 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1586875 | 0.83[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1602671 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1844995 | 0.83[EUR][1000 genomes] |
rs2029636 | 0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2029637 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2046983 | 0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs2087768 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2131233 | 0.94[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2399405 | 0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs28421010 | 0.81[EUR][1000 genomes] |
rs3929356 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs3995955 | 0.85[EUR][1000 genomes] |
rs4352358 | 0.90[ASN][1000 genomes] |
rs4438629 | 0.87[ASN][1000 genomes] |
rs4440096 | 0.82[EUR][1000 genomes] |
rs4449289 | 0.83[EUR][1000 genomes] |
rs4528910 | 0.83[EUR][1000 genomes] |
rs4568109 | 0.83[EUR][1000 genomes] |
rs4568110 | 0.83[EUR][1000 genomes] |
rs4577433 | 0.87[ASN][1000 genomes] |
rs4586779 | 0.87[ASN][1000 genomes] |
rs4682086 | 0.85[ASN][1000 genomes] |
rs4682090 | 0.84[ASN][1000 genomes] |
rs4682361 | 0.81[ASN][1000 genomes] |
rs4682365 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4682372 | 0.90[ASN][1000 genomes] |
rs4682374 | 0.90[ASN][1000 genomes] |
rs4682391 | 0.81[EUR][1000 genomes] |
rs5013874 | 0.83[EUR][1000 genomes] |
rs56852402 | 0.83[EUR][1000 genomes] |
rs60443450 | 0.83[EUR][1000 genomes] |
rs62277462 | 0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62279470 | 0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6438039 | 0.87[ASN][1000 genomes] |
rs6763462 | 0.83[EUR][1000 genomes] |
rs6764248 | 0.85[ASN][1000 genomes] |
rs6766122 | 0.83[EUR][1000 genomes] |
rs6766622 | 0.85[EUR][1000 genomes] |
rs6766996 | 0.87[ASN][1000 genomes] |
rs6767017 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6773161 | 0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6784524 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6791042 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6792318 | 0.83[EUR][1000 genomes] |
rs6801501 | 0.82[EUR][1000 genomes] |
rs6805795 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6807950 | 0.83[EUR][1000 genomes] |
rs6808920 | 0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7611019 | 0.83[EUR][1000 genomes] |
rs7614211 | 0.83[EUR][1000 genomes] |
rs7616020 | 0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7622733 | 0.86[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7642447 | 0.83[EUR][1000 genomes] |
rs7642496 | 0.83[EUR][1000 genomes] |
rs7646742 | 0.83[EUR][1000 genomes] |
rs9288937 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs9288938 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9288943 | 0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs958695 | 0.90[ASN][1000 genomes] |
rs9809196 | 0.83[EUR][1000 genomes] |
rs9818716 | 0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9821935 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9827793 | 0.83[EUR][1000 genomes] |
rs9827894 | 0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9828290 | 0.83[EUR][1000 genomes] |
rs9828502 | 0.81[EUR][1000 genomes] |
rs9829464 | 0.83[EUR][1000 genomes] |
rs9837375 | 0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs9844769 | 0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9851173 | 0.86[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9859163 | 0.83[EUR][1000 genomes] |
rs9861756 | 0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs9864872 | 0.83[EUR][1000 genomes] |
rs9871650 | 0.90[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9872691 | 0.83[EUR][1000 genomes] |
rs9875860 | 0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv10307 | chr3:111903974-112087686 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv591291 | chr3:111914624-111962851 | ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
3 | nsv591292 | chr3:111914624-111993915 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
4 | esv3437811 | chr3:111929311-111950399 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | inside rSNPs | n/a |
5 | nsv877340 | chr3:111936961-112013546 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:111937000-111942800 | Weak transcription | Left Ventricle | heart |