Variant report
| Variant | rs7533486 |
|---|---|
| Chromosome Location | chr1:217302986-217302987 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr1:217301751..217304331-chr1:217305363..217307786,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:19)
| rs_ID | r2[population] |
|---|---|
| rs10158793 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs11117773 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12119709 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12121561 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12121769 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12122960 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12125004 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12125898 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12126433 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12133995 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12135903 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12141781 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17696143 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs41283142 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6674783 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7518540 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7546014 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7550505 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs830304 | 0.82[EUR][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 | nsv428610 | chr1:217143317-217307243 | Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:217298200-217307000 | Weak transcription | Fetal Heart | heart |
