Variant report
| Variant | rs13437462 |
|---|---|
| Chromosome Location | chr6:49986644-49986645 |
| allele | A/G |
| 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)
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(count:2 , 50 per page) page:
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rSNPs within LD-proxies of this variant (count:14)
| rs_ID | r2[population] |
|---|---|
| rs9463564 | 1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs9463565 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs9463568 | 1.00[AMR][1000 genomes] |
| rs9463571 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs9473715 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs9473717 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs9473719 | 1.00[YRI][hapmap] |
| rs9473720 | 1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs9473721 | 1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs9473724 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs9473734 | 1.00[YRI][hapmap] |
| rs9473741 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs9473742 | 1.00[AMR][1000 genomes] |
| rs9885929 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv933942 | chr6:49480550-50004231 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
| 2 | nsv5295 | chr6:49955078-50007710 | Enhancers Active TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
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