Variant report
| Variant | rs2822655 | 
|---|---|
| Chromosome Location | chr21:15766654-15766655 | 
| allele | C/T | 
| Outlinks | Ensembl   UCSC | 
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data | 
| No data | 
          
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| rs_ID | r2[population] | 
|---|---|
| rs1040330 | 0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes] | 
| rs11908970 | 0.86[ASN][1000 genomes] | 
| rs12479 | 0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] | 
| rs13048179 | 0.85[AMR][1000 genomes];0.88[ASN][1000 genomes] | 
| rs13048477 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] | 
| rs2037941 | 0.93[AMR][1000 genomes];0.87[ASN][1000 genomes] | 
| rs2142240 | 0.82[AMR][1000 genomes];0.88[ASN][1000 genomes] | 
| rs2822624 | 0.80[ASN][1000 genomes] | 
| rs2822629 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] | 
| rs2822631 | 0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] | 
| rs2822632 | 0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] | 
| rs2822636 | 0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] | 
| rs2822638 | 0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes] | 
| rs2822642 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] | 
| rs2822644 | 0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] | 
| rs2822652 | 0.84[ASN][1000 genomes] | 
| rs2822662 | 0.86[ASN][1000 genomes] | 
| rs7276170 | 0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] | 
| rs7282521 | 0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] | 
| rs9982492 | 0.85[AMR][1000 genomes];0.88[ASN][1000 genomes] | 
| rs9984779 | 0.81[AMR][1000 genomes];0.90[ASN][1000 genomes] | 
 Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 
                     
                        
                             
                                 
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                      Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 
                     
                        
                             
                                 
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                 | No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits | 
|---|---|---|---|---|---|---|---|
| 1 | nsv1064554 | chr21:15676222-15809321 | Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases | 
| 2 | nsv913403 | chr21:15743387-15786271 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases | 
| No data | 
| No. | Chromosome Location | Chromatin state | Cell line | Tissue | 
|---|---|---|---|---|
| 1 | chr21:15766600-15766800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland | 






