Variant report
Variant | rs10895910 |
---|---|
Chromosome Location | chr11:106018470-106018471 |
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] |
---|---|
rs10736649 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs10750742 | 0.96[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs10750743 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs10750744 | 0.92[ASN][1000 genomes] |
rs10750745 | 0.92[ASN][1000 genomes] |
rs10750746 | 0.82[ASN][1000 genomes] |
rs10750747 | 0.89[ASN][1000 genomes] |
rs10750748 | 0.88[ASN][1000 genomes] |
rs10750749 | 0.88[ASN][1000 genomes] |
rs10750750 | 0.95[CHB][hapmap] |
rs10791783 | 0.88[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs10791784 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs10791785 | 0.95[ASN][1000 genomes] |
rs10791787 | 0.89[ASN][1000 genomes] |
rs10791788 | 0.89[ASN][1000 genomes] |
rs10791789 | 0.88[ASN][1000 genomes] |
rs10791790 | 0.87[ASN][1000 genomes] |
rs10791791 | 0.88[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs10791792 | 0.85[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs10791793 | 0.87[ASN][1000 genomes] |
rs10791794 | 0.85[ASN][1000 genomes] |
rs10791795 | 0.84[ASN][1000 genomes] |
rs10791796 | 0.84[ASN][1000 genomes] |
rs10791797 | 0.84[ASN][1000 genomes] |
rs10791798 | 0.81[ASN][1000 genomes] |
rs10791799 | 0.88[AFR][1000 genomes];0.81[ASN][1000 genomes] |
rs10791800 | 0.81[ASN][1000 genomes] |
rs10791802 | 0.95[CHB][hapmap];0.82[JPT][hapmap];0.85[YRI][hapmap] |
rs10895904 | 0.84[CEU][hapmap];0.81[JPT][hapmap] |
rs10895908 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10895909 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10895912 | 0.93[ASN][1000 genomes] |
rs10895913 | 0.95[ASN][1000 genomes] |
rs10895914 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs10895915 | 0.95[ASN][1000 genomes] |
rs10895917 | 0.94[ASN][1000 genomes] |
rs10895918 | 0.94[ASN][1000 genomes] |
rs10895921 | 0.92[ASN][1000 genomes] |
rs10895922 | 0.92[ASN][1000 genomes] |
rs10895923 | 0.89[ASN][1000 genomes] |
rs10895924 | 0.88[ASN][1000 genomes] |
rs10895925 | 0.88[ASN][1000 genomes] |
rs10895926 | 0.88[ASN][1000 genomes] |
rs10895928 | 0.88[ASN][1000 genomes] |
rs10895929 | 0.92[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs10895930 | 0.88[ASN][1000 genomes] |
rs10895931 | 0.87[ASN][1000 genomes] |
rs10895932 | 0.84[ASN][1000 genomes] |
rs10895938 | 0.85[AFR][1000 genomes] |
rs11226922 | 0.86[JPT][hapmap] |
rs11226939 | 0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11226942 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs11226946 | 0.90[AFR][1000 genomes];0.83[ASN][1000 genomes] |
rs11226947 | 0.89[ASN][1000 genomes] |
rs11226982 | 0.85[AFR][1000 genomes] |
rs12225407 | 0.88[AFR][1000 genomes] |
rs1354986 | 0.90[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs1359144 | 0.95[ASN][1000 genomes] |
rs1396156 | 0.95[CHB][hapmap];0.82[JPT][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes] |
rs1605566 | 0.85[AFR][1000 genomes] |
rs1605567 | 0.95[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes] |
rs1806481 | 1.00[ASW][hapmap];0.95[CHB][hapmap];0.81[CHD][hapmap];0.82[JPT][hapmap];0.83[LWK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes] |
rs1893171 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs1893854 | 0.83[ASN][1000 genomes] |
rs1893855 | 0.84[ASN][1000 genomes] |
rs1893857 | 0.84[ASN][1000 genomes] |
rs1939798 | 0.84[CEU][hapmap];0.86[JPT][hapmap] |
rs1939799 | 0.84[CEU][hapmap];0.81[JPT][hapmap] |
rs1939807 | 0.88[ASN][1000 genomes] |
rs1939808 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1940756 | 0.97[ASN][1000 genomes] |
rs1940758 | 0.87[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs1940759 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs1940760 | 0.96[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs1940765 | 0.87[ASN][1000 genomes] |
rs1940766 | 0.85[ASN][1000 genomes] |
rs1940767 | 0.88[ASN][1000 genomes] |
rs1940777 | 0.84[ASN][1000 genomes] |
rs1940778 | 0.84[ASN][1000 genomes] |
rs1940779 | 0.84[ASN][1000 genomes] |
rs1940780 | 0.83[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs1940782 | 0.83[ASN][1000 genomes] |
rs1940783 | 0.83[ASN][1000 genomes] |
rs1940785 | 0.95[ASN][1000 genomes] |
rs1940786 | 0.95[ASN][1000 genomes] |
rs1940787 | 0.95[ASN][1000 genomes] |
rs1940790 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1944772 | 0.84[ASN][1000 genomes] |
rs1944774 | 0.81[ASN][1000 genomes] |
rs1944775 | 0.81[ASN][1000 genomes] |
rs2096833 | 0.92[ASN][1000 genomes] |
rs2155340 | 0.84[CEU][hapmap];0.81[JPT][hapmap] |
rs2155649 | 0.88[ASN][1000 genomes] |
rs2155650 | 0.87[ASN][1000 genomes] |
rs2155652 | 0.84[ASN][1000 genomes] |
rs2155653 | 0.84[ASN][1000 genomes] |
rs2186731 | 0.84[CEU][hapmap];0.81[JPT][hapmap] |
rs2186880 | 0.88[ASN][1000 genomes] |
rs4237619 | 0.94[ASN][1000 genomes] |
rs4237620 | 0.95[ASN][1000 genomes] |
rs4237621 | 0.92[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs4298866 | 0.95[ASN][1000 genomes] |
rs4310571 | 0.89[ASN][1000 genomes] |
rs4365018 | 0.87[ASN][1000 genomes] |
rs4366457 | 0.92[ASN][1000 genomes] |
rs4373882 | 0.88[ASN][1000 genomes] |
rs4431993 | 0.87[ASN][1000 genomes] |
rs4440991 | 0.81[JPT][hapmap] |
rs4475893 | 0.81[ASN][1000 genomes] |
rs4477412 | 0.92[ASN][1000 genomes] |
rs4486594 | 0.94[ASN][1000 genomes] |
rs4488166 | 0.89[ASN][1000 genomes] |
rs4505036 | 0.92[ASN][1000 genomes] |
rs4505037 | 0.92[ASN][1000 genomes] |
rs4506615 | 0.95[ASN][1000 genomes] |
rs4508178 | 0.87[ASN][1000 genomes] |
rs4512783 | 0.88[ASN][1000 genomes] |
rs4512788 | 0.87[ASN][1000 genomes] |
rs4514384 | 0.92[ASN][1000 genomes] |
rs4529863 | 0.92[ASN][1000 genomes] |
rs4558141 | 0.84[ASN][1000 genomes] |
rs4559652 | 0.88[ASN][1000 genomes] |
rs4754141 | 0.84[CEU][hapmap];0.81[JPT][hapmap] |
rs4754146 | 0.94[ASN][1000 genomes] |
rs4754147 | 0.94[ASN][1000 genomes] |
rs4754148 | 0.95[ASN][1000 genomes] |
rs4754151 | 0.87[ASN][1000 genomes] |
rs4755127 | 0.95[ASN][1000 genomes] |
rs4755128 | 0.95[ASN][1000 genomes] |
rs4755129 | 0.88[ASN][1000 genomes] |
rs4755130 | 0.86[ASN][1000 genomes] |
rs4755134 | 0.88[ASN][1000 genomes] |
rs4755137 | 0.87[ASN][1000 genomes] |
rs4755138 | 0.87[ASN][1000 genomes] |
rs4755140 | 0.92[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs4755146 | 0.95[CHB][hapmap] |
rs5019762 | 0.90[AFR][1000 genomes];0.81[ASN][1000 genomes] |
rs602407 | 0.81[CHB][hapmap] |
rs674799 | 0.81[CHB][hapmap] |
rs7110907 | 0.84[ASN][1000 genomes] |
rs7112436 | 0.96[AFR][1000 genomes];0.92[ASN][1000 genomes] |
rs7115529 | 0.92[ASN][1000 genomes] |
rs7126811 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs754562 | 0.84[CEU][hapmap];0.85[JPT][hapmap] |
rs766717 | 0.84[CEU][hapmap];0.86[JPT][hapmap] |
rs7934227 | 0.96[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs7943598 | 0.92[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs7947817 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1048381 | chr11:105945117-106561574 | Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
2 | nsv898358 | chr11:105999580-106182251 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv430428 | chr11:106005901-106173046 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:106016400-106019200 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |