Variant report
| Variant | rs10030923 |
|---|---|
| Chromosome Location | chr4:150005053-150005054 |
| allele | A/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 |
rSNPs within LD-proxies of this variant (count:35)
| rs_ID | r2[population] |
|---|---|
| rs10001238 | 1.00[AMR][1000 genomes] |
| rs10002382 | 1.00[AMR][1000 genomes] |
| rs10008213 | 1.00[AMR][1000 genomes] |
| rs10020031 | 1.00[AMR][1000 genomes] |
| rs10021342 | 1.00[AMR][1000 genomes] |
| rs10022699 | 1.00[AMR][1000 genomes] |
| rs10024710 | 1.00[AMR][1000 genomes] |
| rs10028420 | 1.00[AMR][1000 genomes] |
| rs10028781 | 1.00[AMR][1000 genomes] |
| rs10034293 | 1.00[AMR][1000 genomes] |
| rs10035071 | 1.00[AMR][1000 genomes] |
| rs10471066 | 1.00[AMR][1000 genomes] |
| rs10471067 | 1.00[AMR][1000 genomes] |
| rs28380503 | 1.00[AMR][1000 genomes] |
| rs28474774 | 1.00[AMR][1000 genomes] |
| rs28507209 | 1.00[AMR][1000 genomes] |
| rs28547154 | 1.00[AMR][1000 genomes] |
| rs28556844 | 1.00[AMR][1000 genomes] |
| rs28565297 | 1.00[AMR][1000 genomes] |
| rs28578645 | 1.00[AMR][1000 genomes] |
| rs28597972 | 1.00[AMR][1000 genomes] |
| rs28599473 | 1.00[AMR][1000 genomes] |
| rs28611497 | 1.00[AMR][1000 genomes] |
| rs28682907 | 1.00[AMR][1000 genomes] |
| rs28690552 | 1.00[AMR][1000 genomes] |
| rs28691729 | 1.00[AMR][1000 genomes] |
| rs28749928 | 1.00[AMR][1000 genomes] |
| rs28753681 | 1.00[AMR][1000 genomes] |
| rs6834249 | 1.00[AMR][1000 genomes] |
| rs73857868 | 1.00[AMR][1000 genomes] |
| rs73857869 | 1.00[AMR][1000 genomes] |
| rs9992862 | 1.00[AMR][1000 genomes] |
| rs9994392 | 1.00[AMR][1000 genomes] |
| rs9997937 | 1.00[AMR][1000 genomes] |
| rs9999957 | 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 | nsv4544 | chr4:149979800-150026323 | Weak transcription Enhancers Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr4:150004200-150005200 | Enhancers | Adipose Nuclei | Adipose |
