Variant report
Variant | rs11916841 |
---|---|
Chromosome Location | chr3:94868683-94868684 |
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] |
---|---|
rs10511151 | 0.81[EUR][1000 genomes] |
rs10933902 | 1.00[ASN][1000 genomes] |
rs10933932 | 0.89[ASN][1000 genomes] |
rs10933940 | 0.80[ASN][1000 genomes] |
rs10933941 | 0.82[ASN][1000 genomes] |
rs10933955 | 0.80[ASN][1000 genomes] |
rs11708513 | 0.82[EUR][1000 genomes] |
rs11708877 | 1.00[ASN][1000 genomes] |
rs11708909 | 0.82[EUR][1000 genomes] |
rs11712473 | 0.82[EUR][1000 genomes] |
rs11712965 | 0.82[EUR][1000 genomes] |
rs11713390 | 0.81[EUR][1000 genomes] |
rs11713740 | 0.98[ASN][1000 genomes] |
rs11713846 | 0.82[EUR][1000 genomes] |
rs11715007 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11719105 | 1.00[ASN][1000 genomes] |
rs11918166 | 0.88[ASN][1000 genomes] |
rs11923227 | 0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11923257 | 0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11923675 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11923716 | 0.89[ASN][1000 genomes] |
rs11923738 | 0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs11925057 | 0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12486859 | 0.81[EUR][1000 genomes] |
rs12496724 | 0.81[ASN][1000 genomes] |
rs12630013 | 0.82[ASN][1000 genomes] |
rs12630818 | 1.00[ASN][1000 genomes] |
rs12630859 | 0.82[ASN][1000 genomes] |
rs12631889 | 0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12634496 | 0.98[ASN][1000 genomes] |
rs12695188 | 0.81[EUR][1000 genomes] |
rs13066378 | 0.80[ASN][1000 genomes] |
rs13070939 | 0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs13075156 | 0.89[AFR][1000 genomes] |
rs13081547 | 0.80[ASN][1000 genomes] |
rs13091172 | 0.81[ASN][1000 genomes] |
rs1356269 | 0.80[ASN][1000 genomes] |
rs1432468 | 0.84[CEU][hapmap] |
rs1476323 | 0.82[ASN][1000 genomes] |
rs1516601 | 0.81[EUR][1000 genomes] |
rs17383687 | 0.82[ASN][1000 genomes] |
rs17383861 | 0.82[ASN][1000 genomes] |
rs17384029 | 0.80[ASN][1000 genomes] |
rs17384064 | 0.82[ASN][1000 genomes] |
rs17442941 | 0.82[ASN][1000 genomes] |
rs17497733 | 0.99[ASN][1000 genomes] |
rs1914063 | 0.81[ASN][1000 genomes] |
rs1968016 | 0.82[ASN][1000 genomes] |
rs2048861 | 0.82[ASN][1000 genomes] |
rs2048863 | 0.80[ASN][1000 genomes] |
rs2176276 | 0.80[ASN][1000 genomes] |
rs2310403 | 0.89[ASN][1000 genomes] |
rs2310406 | 0.88[ASN][1000 genomes] |
rs3849443 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3905401 | 0.95[ASN][1000 genomes] |
rs3907753 | 0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3926894 | 0.82[ASN][1000 genomes] |
rs4132577 | 0.84[EUR][1000 genomes] |
rs4535228 | 0.80[ASN][1000 genomes] |
rs4610223 | 0.89[ASN][1000 genomes] |
rs4857019 | 0.82[EUR][1000 genomes] |
rs4857020 | 0.80[EUR][1000 genomes] |
rs4857157 | 0.82[ASN][1000 genomes] |
rs4857159 | 0.82[ASN][1000 genomes] |
rs56233996 | 0.82[ASN][1000 genomes] |
rs57291530 | 0.82[ASN][1000 genomes] |
rs58549043 | 0.82[EUR][1000 genomes] |
rs58743887 | 0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs58977036 | 0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs59007421 | 0.82[ASN][1000 genomes] |
rs59469832 | 0.81[ASN][1000 genomes] |
rs60875944 | 0.81[ASN][1000 genomes] |
rs61446477 | 0.82[ASN][1000 genomes] |
rs6774134 | 0.82[ASN][1000 genomes] |
rs67828560 | 0.82[EUR][1000 genomes] |
rs6803510 | 0.89[AFR][1000 genomes] |
rs6806247 | 0.89[AFR][1000 genomes] |
rs6806586 | 0.89[AFR][1000 genomes] |
rs6810229 | 0.82[ASN][1000 genomes] |
rs72615781 | 1.00[ASN][1000 genomes] |
rs72615782 | 1.00[ASN][1000 genomes] |
rs72615787 | 0.96[ASN][1000 genomes] |
rs72615791 | 0.89[ASN][1000 genomes] |
rs72618497 | 0.80[ASN][1000 genomes] |
rs72618498 | 0.82[ASN][1000 genomes] |
rs72618499 | 0.82[ASN][1000 genomes] |
rs72618500 | 0.82[ASN][1000 genomes] |
rs72620004 | 0.82[ASN][1000 genomes] |
rs72620005 | 0.82[ASN][1000 genomes] |
rs72620006 | 0.81[ASN][1000 genomes] |
rs72620007 | 0.81[ASN][1000 genomes] |
rs7619484 | 0.82[EUR][1000 genomes] |
rs7620952 | 0.89[AFR][1000 genomes] |
rs7622398 | 0.82[CEU][hapmap] |
rs7628826 | 0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7634250 | 0.84[EUR][1000 genomes] |
rs7639829 | 0.82[ASN][1000 genomes] |
rs9288845 | 0.82[EUR][1000 genomes] |
rs9288846 | 0.82[EUR][1000 genomes] |
rs9809394 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9812403 | 0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9815317 | 0.89[AFR][1000 genomes] |
rs9820431 | 0.89[AFR][1000 genomes] |
rs9825156 | 0.82[EUR][1000 genomes] |
rs9832182 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9842570 | 0.81[EUR][1000 genomes] |
rs9845130 | 0.82[EUR][1000 genomes] |
rs9847352 | 0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9855703 | 0.81[EUR][1000 genomes] |
rs9864255 | 0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9868858 | 0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9878073 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1013680 | chr3:94777881-95538336 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv536653 | chr3:94777881-95538336 | Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv877170 | chr3:94790666-95564838 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv877171 | chr3:94797731-94909337 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv877172 | chr3:94807394-94943493 | Enhancers Weak transcription Active TSS ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv877173 | chr3:94813120-94904714 | Enhancers ZNF genes & repeats Weak transcription | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv999347 | chr3:94832290-95177750 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv460765 | chr3:94837728-94904714 | Weak transcription Enhancers ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
9 | nsv590994 | chr3:94837728-94904714 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
10 | nsv590995 | chr3:94841342-94918524 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
11 | nsv590996 | chr3:94857157-94914290 | Enhancers Weak transcription | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
12 | nsv590997 | chr3:94865957-94918524 | Weak transcription Enhancers | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
13 | nsv877174 | chr3:94867122-94983900 | Enhancers Weak transcription ZNF genes & repeats Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
14 | esv2754985 | chr3:94868320-94970627 | Enhancers Active TSS Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:94865200-94870400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
2 | chr3:94865200-94870400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr3:94865200-94870400 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
4 | chr3:94865400-94870400 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |