Variant report
| Variant | rs4675767 |
|---|---|
| Chromosome Location | chr2:209312771-209312772 |
| 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:15)
| rs_ID | r2[population] |
|---|---|
| rs1023751 | 1.00[AMR][1000 genomes] |
| rs10755022 | 1.00[AMR][1000 genomes] |
| rs10932258 | 1.00[AMR][1000 genomes] |
| rs11690008 | 1.00[AMR][1000 genomes] |
| rs12474810 | 1.00[AMR][1000 genomes] |
| rs1529978 | 1.00[AMR][1000 genomes] |
| rs1992740 | 1.00[AMR][1000 genomes] |
| rs2043718 | 1.00[AMR][1000 genomes] |
| rs2043719 | 1.00[AMR][1000 genomes] |
| rs2118298 | 1.00[AMR][1000 genomes] |
| rs2363464 | 1.00[AMR][1000 genomes] |
| rs4675756 | 1.00[AMR][1000 genomes] |
| rs6435438 | 1.00[AMR][1000 genomes] |
| rs6755550 | 1.00[AMR][1000 genomes] |
| rs7593482 | 1.00[AMR][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 | nsv584297 | chr2:209020181-209316760 | Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
