Variant report
Variant | rs10792715 |
---|---|
Chromosome Location | chr11:83783388-83783389 |
allele | C/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] |
---|---|
rs10792712 | 0.82[AMR][1000 genomes] |
rs10792713 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10792714 | 0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10792716 | 1.00[ASN][1000 genomes] |
rs10792717 | 0.98[ASN][1000 genomes] |
rs10792718 | 1.00[ASN][1000 genomes] |
rs10898195 | 0.94[ASN][1000 genomes] |
rs10898196 | 0.86[ASN][1000 genomes] |
rs10898197 | 0.89[ASN][1000 genomes] |
rs10898198 | 0.97[ASN][1000 genomes] |
rs10898202 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11233894 | 0.85[ASN][1000 genomes] |
rs11233900 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11602701 | 0.95[ASN][1000 genomes] |
rs12363188 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12574301 | 0.95[ASN][1000 genomes] |
rs12575314 | 0.95[ASN][1000 genomes] |
rs12577433 | 0.95[ASN][1000 genomes] |
rs12806160 | 0.82[ASN][1000 genomes] |
rs1573569 | 0.97[ASN][1000 genomes] |
rs1573570 | 0.94[ASN][1000 genomes] |
rs1573571 | 0.97[ASN][1000 genomes] |
rs1573574 | 1.00[ASN][1000 genomes] |
rs1894171 | 0.95[ASN][1000 genomes] |
rs1894172 | 0.95[ASN][1000 genomes] |
rs1945799 | 0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1945800 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1945801 | 0.91[ASN][1000 genomes] |
rs1945804 | 0.82[AMR][1000 genomes] |
rs1945807 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs1945809 | 0.86[ASN][1000 genomes] |
rs1945813 | 0.82[ASN][1000 genomes] |
rs1945814 | 0.84[ASN][1000 genomes] |
rs1945815 | 0.82[AMR][1000 genomes] |
rs1945830 | 1.00[ASN][1000 genomes] |
rs1945832 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1984374 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2032401 | 1.00[ASN][1000 genomes] |
rs2051472 | 0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3750917 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs3905309 | 0.95[ASN][1000 genomes] |
rs4322419 | 0.97[ASN][1000 genomes] |
rs4586191 | 0.82[ASN][1000 genomes] |
rs4943885 | 0.82[ASN][1000 genomes] |
rs4943886 | 0.95[ASN][1000 genomes] |
rs4944460 | 0.82[ASN][1000 genomes] |
rs4944461 | 0.95[ASN][1000 genomes] |
rs4944462 | 0.95[ASN][1000 genomes] |
rs4944463 | 1.00[ASN][1000 genomes] |
rs4944464 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6592158 | 0.94[ASN][1000 genomes] |
rs6592159 | 0.94[ASN][1000 genomes] |
rs6592163 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7108711 | 0.97[ASN][1000 genomes] |
rs7109671 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7114926 | 0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7122677 | 0.97[ASN][1000 genomes] |
rs7122855 | 0.97[ASN][1000 genomes] |
rs7122967 | 0.97[ASN][1000 genomes] |
rs7123054 | 0.95[ASN][1000 genomes] |
rs7126268 | 0.97[ASN][1000 genomes] |
rs7924360 | 0.95[ASN][1000 genomes] |
rs7924443 | 0.95[ASN][1000 genomes] |
rs7924476 | 0.95[ASN][1000 genomes] |
rs7924503 | 0.95[ASN][1000 genomes] |
rs7924835 | 0.95[ASN][1000 genomes] |
rs7927619 | 0.95[ASN][1000 genomes] |
rs7928752 | 0.82[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs7929774 | 0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7930853 | 0.85[EUR][1000 genomes] |
rs7935399 | 0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7936419 | 0.84[ASN][1000 genomes] |
rs7951507 | 0.85[ASN][1000 genomes] |
rs7952161 | 0.94[ASN][1000 genomes] |
rs7952171 | 0.95[ASN][1000 genomes] |
rs7952399 | 0.95[ASN][1000 genomes] |
rs7952517 | 0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv898025 | chr11:83658909-83796678 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
2 | nsv1039924 | chr11:83662904-83993497 | Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv541102 | chr11:83662904-83993497 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv898026 | chr11:83685801-83789540 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
5 | esv1809938 | chr11:83716145-83789540 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
6 | nsv898027 | chr11:83717887-83798485 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
7 | nsv898028 | chr11:83717887-83817360 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
8 | nsv898029 | chr11:83717887-83939591 | Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
9 | nsv898030 | chr11:83730570-83789540 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:83781000-83784200 | Weak transcription | Brain Anterior Caudate | brain |
2 | chr11:83781200-83787400 | Weak transcription | Brain Angular Gyrus | brain |
3 | chr11:83781400-83794400 | Weak transcription | Brain Cingulate Gyrus | brain |
4 | chr11:83781800-83787200 | Weak transcription | Brain Inferior Temporal Lobe | brain |
5 | chr11:83782000-83783400 | Weak transcription | Brain Substantia Nigra | brain |
6 | chr11:83783200-83783600 | Enhancers | Brain Hippocampus Middle | brain |