Variant report
| Variant | rs2232570 |
|---|---|
| Chromosome Location | chr12:48961981-48961982 |
| 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 |
rSNPs within LD-proxies of this variant (count:27)
| rs_ID | r2[population] |
|---|---|
| rs10783256 | 1.00[CHB][hapmap] |
| rs11168576 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
| rs11168628 | 0.86[ASN][1000 genomes] |
| rs11168629 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs11168630 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs11168631 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs11168632 | 0.86[ASN][1000 genomes] |
| rs11168633 | 0.86[ASN][1000 genomes] |
| rs11168634 | 1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs11168635 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs11168636 | 1.00[CHB][hapmap];0.86[ASN][1000 genomes] |
| rs11168638 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs11168639 | 0.86[ASN][1000 genomes] |
| rs11168640 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
| rs12229098 | 0.86[ASN][1000 genomes] |
| rs12230091 | 0.86[ASN][1000 genomes] |
| rs12230448 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs12230471 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs17237094 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
| rs17237198 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
| rs17834022 | 1.00[CHB][hapmap] |
| rs2468942 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
| rs2705123 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
| rs2705126 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
| rs2731073 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
| rs2731101 | 1.00[CHB][hapmap] |
| rs61995742 | 0.93[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv427911 | chr12:48670336-48979396 | Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 35 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
