Variant report
| Variant | rs2822577 | 
|---|---|
| Chromosome Location | chr21:15705554-15705555 | 
| 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] | 
|---|---|
| rs1153323 | 0.82[CHD][hapmap] | 
| rs1153329 | 0.82[CHD][hapmap] | 
| rs1297151 | 0.95[CHB][hapmap];1.00[JPT][hapmap] | 
| rs2205254 | 0.88[ASN][1000 genomes] | 
| rs2245589 | 0.82[CHB][hapmap];0.95[JPT][hapmap] | 
| rs2403770 | 0.82[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.82[ASN][1000 genomes] | 
| rs2822564 | 0.91[CEU][hapmap] | 
| rs2822580 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap] | 
| rs2822582 | 0.87[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.95[MEX][hapmap];0.81[MKK][hapmap];0.88[YRI][hapmap] | 
| rs4387887 | 0.82[CHB][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap] | 
| rs887768 | 0.82[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes] | 
| rs887773 | 0.82[CHD][hapmap] | 
 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 | nsv1066930 | chr21:15626232-15724630 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases | 
| 2 | 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 | 
| No data | 






