Variant report
| Variant | rs56689123 | 
|---|---|
| Chromosome Location | chr21:15952178-15952179 | 
| allele | A/C | 
| Outlinks | Ensembl   UCSC | 
- TF binding region (count:2)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
            
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| Variant related genes | Relation type | 
|---|---|
| SAMSN1-AS1 | TF binding region | 
| rs_ID | r2[population] | 
|---|---|
| rs57061183 | 1.00[ASN][1000 genomes] | 
| rs57285749 | 1.00[ASN][1000 genomes] | 
| rs57460587 | 1.00[ASN][1000 genomes] | 
| rs58907859 | 1.00[ASN][1000 genomes] | 
| rs58995566 | 1.00[ASN][1000 genomes] | 
| rs59196713 | 1.00[ASN][1000 genomes] | 
| rs60267968 | 1.00[ASN][1000 genomes] | 
| rs61244737 | 1.00[ASN][1000 genomes] | 
| rs7275458 | 1.00[ASN][1000 genomes] | 
| rs7278813 | 1.00[ASN][1000 genomes] | 
| rs73344137 | 1.00[ASN][1000 genomes] | 
| rs73344139 | 1.00[ASN][1000 genomes] | 
| rs8127259 | 1.00[ASN][1000 genomes] | 
| rs8127264 | 1.00[ASN][1000 genomes] | 
| rs8131133 | 1.00[ASN][1000 genomes] | 
| rs8131837 | 1.00[ASN][1000 genomes] | 
| rs8133615 | 1.00[ASN][1000 genomes] | 
| rs9977981 | 1.00[ASN][1000 genomes] | 
 Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 
                     
                        
                             
                                 
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                      Variant overlapped rSNPs/rCNVs (count:5 , 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 | nsv1059591 | chr21:15835325-15969195 | Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases | 
| 2 | nsv1057934 | chr21:15863224-15969195 | Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases | 
| 3 | nsv834045 | chr21:15900678-16112850 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases | 
| 4 | nsv834046 | chr21:15903792-16077369 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases | 
| 5 | nsv470879 | chr21:15946828-15964278 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases | 
| No data | 
| No. | Chromosome Location | Chromatin state | Cell line | Tissue | 
|---|---|---|---|---|
| 1 | chr21:15952000-15953400 | Enhancers | K562 | blood | 






