Variant report
Variant | rs4694603 |
---|---|
Chromosome Location | chr4:69936715-69936716 |
allele | A/C |
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] |
---|---|
rs10006452 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs11249521 | 0.81[EUR][1000 genomes] |
rs11249522 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11249523 | 0.83[EUR][1000 genomes] |
rs11249524 | 0.83[EUR][1000 genomes] |
rs11249526 | 0.82[EUR][1000 genomes] |
rs11249527 | 0.82[EUR][1000 genomes] |
rs11249528 | 0.82[EUR][1000 genomes] |
rs11931182 | 0.83[EUR][1000 genomes] |
rs11932131 | 0.82[EUR][1000 genomes] |
rs11934762 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs11935886 | 0.81[EUR][1000 genomes] |
rs11936822 | 0.80[EUR][1000 genomes] |
rs11940220 | 0.82[EUR][1000 genomes] |
rs11940316 | 0.81[EUR][1000 genomes] |
rs12506962 | 0.82[EUR][1000 genomes] |
rs12508257 | 0.82[EUR][1000 genomes] |
rs12512526 | 0.82[EUR][1000 genomes] |
rs12513195 | 0.82[EUR][1000 genomes] |
rs12642938 | 0.81[EUR][1000 genomes] |
rs12643840 | 0.83[EUR][1000 genomes] |
rs12646327 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12647434 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12647681 | 0.82[EUR][1000 genomes] |
rs12647682 | 0.82[EUR][1000 genomes] |
rs28375964 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs28712409 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs34318523 | 0.82[EUR][1000 genomes] |
rs34386959 | 0.82[EUR][1000 genomes] |
rs34630750 | 0.82[EUR][1000 genomes] |
rs35297888 | 0.82[EUR][1000 genomes] |
rs3924192 | 0.82[EUR][1000 genomes] |
rs4131317 | 0.83[EUR][1000 genomes] |
rs4273534 | 0.83[EUR][1000 genomes] |
rs4293848 | 0.82[EUR][1000 genomes] |
rs4307027 | 0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4309908 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4314345 | 0.81[EUR][1000 genomes] |
rs4337789 | 0.82[EUR][1000 genomes] |
rs4351080 | 0.82[EUR][1000 genomes] |
rs4356974 | 0.82[EUR][1000 genomes] |
rs4364327 | 0.81[EUR][1000 genomes] |
rs4371687 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4371688 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4443355 | 0.83[EUR][1000 genomes] |
rs4446391 | 0.82[EUR][1000 genomes] |
rs4454000 | 0.83[EUR][1000 genomes] |
rs4455491 | 0.82[EUR][1000 genomes] |
rs4458521 | 0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4478248 | 0.83[EUR][1000 genomes] |
rs4516790 | 0.88[ASN][1000 genomes] |
rs4521414 | 0.81[EUR][1000 genomes] |
rs4522933 | 0.83[EUR][1000 genomes] |
rs4540108 | 0.83[EUR][1000 genomes] |
rs4541594 | 0.82[EUR][1000 genomes] |
rs4554144 | 0.82[EUR][1000 genomes] |
rs4587017 | 0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4588522 | 0.81[EUR][1000 genomes] |
rs4632729 | 0.83[EUR][1000 genomes] |
rs4640729 | 0.83[EUR][1000 genomes] |
rs4642304 | 0.83[EUR][1000 genomes] |
rs4694169 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4694171 | 0.83[EUR][1000 genomes] |
rs4694591 | 0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4694596 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs5013211 | 0.82[EUR][1000 genomes] |
rs55757747 | 0.83[EUR][1000 genomes] |
rs55834557 | 0.82[EUR][1000 genomes] |
rs56217918 | 0.83[EUR][1000 genomes] |
rs56388229 | 0.81[EUR][1000 genomes] |
rs57216626 | 0.81[EUR][1000 genomes] |
rs58544196 | 0.82[EUR][1000 genomes] |
rs59415892 | 0.82[EUR][1000 genomes] |
rs62296922 | 0.83[EUR][1000 genomes] |
rs62296935 | 0.83[EUR][1000 genomes] |
rs62296936 | 0.83[EUR][1000 genomes] |
rs62296942 | 0.82[EUR][1000 genomes] |
rs62296943 | 0.82[EUR][1000 genomes] |
rs62296944 | 0.82[EUR][1000 genomes] |
rs6422323 | 0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6422324 | 0.83[EUR][1000 genomes] |
rs6422325 | 0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6600866 | 0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6600874 | 0.83[EUR][1000 genomes] |
rs6600875 | 0.82[EUR][1000 genomes] |
rs6600876 | 0.83[EUR][1000 genomes] |
rs6600877 | 0.83[EUR][1000 genomes] |
rs6600878 | 0.82[EUR][1000 genomes] |
rs6600879 | 0.82[EUR][1000 genomes] |
rs6600880 | 0.82[EUR][1000 genomes] |
rs6600883 | 0.82[EUR][1000 genomes] |
rs6600884 | 0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs6600885 | 0.82[EUR][1000 genomes] |
rs6600886 | 0.82[EUR][1000 genomes] |
rs6600887 | 0.82[EUR][1000 genomes] |
rs6600888 | 0.82[EUR][1000 genomes] |
rs6600890 | 0.81[EUR][1000 genomes] |
rs6600891 | 0.82[EUR][1000 genomes] |
rs6600893 | 0.80[EUR][1000 genomes] |
rs6820734 | 0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6830368 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6843382 | 0.83[EUR][1000 genomes] |
rs6846298 | 0.82[EUR][1000 genomes] |
rs6851282 | 0.81[EUR][1000 genomes] |
rs6851533 | 0.80[EUR][1000 genomes] |
rs6858558 | 0.82[EUR][1000 genomes] |
rs7375178 | 0.82[EUR][1000 genomes] |
rs7434332 | 0.82[EUR][1000 genomes] |
rs7437039 | 0.82[EUR][1000 genomes] |
rs7437174 | 0.82[EUR][1000 genomes] |
rs7438135 | 0.82[EUR][1000 genomes] |
rs7438244 | 0.82[EUR][1000 genomes] |
rs7439098 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7439152 | 0.82[EUR][1000 genomes] |
rs7439326 | 0.82[EUR][1000 genomes] |
rs7439792 | 0.82[EUR][1000 genomes] |
rs7441750 | 0.81[EUR][1000 genomes] |
rs7441774 | 0.82[EUR][1000 genomes] |
rs7442453 | 0.82[EUR][1000 genomes] |
rs7442486 | 0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7657423 | 0.82[EUR][1000 genomes] |
rs7658752 | 0.80[EUR][1000 genomes] |
rs7659306 | 0.83[EUR][1000 genomes] |
rs7662029 | 0.82[EUR][1000 genomes] |
rs7663584 | 0.83[EUR][1000 genomes] |
rs7666195 | 0.80[EUR][1000 genomes] |
rs7668258 | 0.82[EUR][1000 genomes] |
rs7674851 | 0.83[EUR][1000 genomes] |
rs7676472 | 0.83[EUR][1000 genomes] |
rs7677611 | 0.83[EUR][1000 genomes] |
rs7678656 | 0.82[EUR][1000 genomes] |
rs7679184 | 0.82[EUR][1000 genomes] |
rs7679550 | 0.83[EUR][1000 genomes] |
rs7680709 | 0.83[EUR][1000 genomes] |
rs7681790 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7685151 | 0.80[EUR][1000 genomes] |
rs7698645 | 0.82[EUR][1000 genomes] |
rs7698846 | 0.82[EUR][1000 genomes] |
rs7699711 | 0.82[EUR][1000 genomes] |
rs7699955 | 0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs9999076 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999654 | chr4:69661415-70132110 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
2 | esv3420586 | chr4:69680878-70322918 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 41 gene(s) | inside rSNPs | diseases |
3 | nsv1067773 | chr4:69718248-70715727 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
4 | esv3468151 | chr4:69718675-70322776 | Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
5 | esv3468153 | chr4:69718675-70322776 | Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
6 | nsv594582 | chr4:69827340-69988378 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
7 | nsv879379 | chr4:69878929-69987249 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
8 | nsv594583 | chr4:69928642-69988378 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv427683 | chr4:69929701-70414172 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
10 | nsv522091 | chr4:69932587-69988378 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv999858 | chr4:69933262-70676525 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:69930600-69944400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr4:69934400-69939200 | Enhancers | Liver | Liver |
3 | chr4:69936400-69938200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr4:69936600-69937200 | Enhancers | HepG2 | liver |