Variant report
| Variant | rs28579751 |
|---|---|
| Chromosome Location | chr4:149997142-149997143 |
| allele | A/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:38)
| rs_ID | r2[population] |
|---|---|
| rs10003214 | 1.00[ASN][1000 genomes] |
| rs10019546 | 1.00[ASN][1000 genomes] |
| rs10021639 | 1.00[ASN][1000 genomes] |
| rs10031956 | 1.00[ASN][1000 genomes] |
| rs10489051 | 1.00[ASN][1000 genomes] |
| rs10489054 | 1.00[ASN][1000 genomes] |
| rs13112975 | 1.00[ASN][1000 genomes] |
| rs13133607 | 1.00[ASN][1000 genomes] |
| rs1438777 | 1.00[ASN][1000 genomes] |
| rs17025376 | 1.00[ASN][1000 genomes] |
| rs17025396 | 1.00[ASN][1000 genomes] |
| rs17725791 | 1.00[ASN][1000 genomes] |
| rs17778070 | 1.00[ASN][1000 genomes] |
| rs2157932 | 1.00[ASN][1000 genomes] |
| rs28394720 | 1.00[ASN][1000 genomes] |
| rs28417942 | 1.00[ASN][1000 genomes] |
| rs28478129 | 1.00[ASN][1000 genomes] |
| rs28491207 | 1.00[ASN][1000 genomes] |
| rs28498848 | 1.00[ASN][1000 genomes] |
| rs28544066 | 1.00[ASN][1000 genomes] |
| rs28557410 | 1.00[ASN][1000 genomes] |
| rs28636985 | 1.00[ASN][1000 genomes] |
| rs28787362 | 1.00[ASN][1000 genomes] |
| rs28860488 | 1.00[ASN][1000 genomes] |
| rs66979066 | 1.00[ASN][1000 genomes] |
| rs67997931 | 1.00[ASN][1000 genomes] |
| rs6835584 | 1.00[ASN][1000 genomes] |
| rs6836835 | 1.00[ASN][1000 genomes] |
| rs6846370 | 1.00[ASN][1000 genomes] |
| rs6854049 | 1.00[ASN][1000 genomes] |
| rs72719869 | 1.00[ASN][1000 genomes] |
| rs756862 | 1.00[ASN][1000 genomes] |
| rs7665428 | 1.00[ASN][1000 genomes] |
| rs7676142 | 1.00[ASN][1000 genomes] |
| rs7676393 | 1.00[ASN][1000 genomes] |
| rs7688521 | 1.00[ASN][1000 genomes] |
| rs9992331 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs9994141 | 1.00[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 | 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 | chr4:149996800-149997400 | Weak transcription | Psoas Muscle | Psoas |
