Variant report
| Variant | rs4511667 |
|---|---|
| Chromosome Location | chr2:141285184-141285185 |
| 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:15)
| rs_ID | r2[population] |
|---|---|
| rs11890379 | 0.95[YRI][hapmap] |
| rs11899209 | 1.00[EUR][1000 genomes] |
| rs13404083 | 0.91[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs16843953 | 1.00[EUR][1000 genomes] |
| rs16843971 | 1.00[EUR][1000 genomes] |
| rs16843973 | 1.00[EUR][1000 genomes] |
| rs16843986 | 1.00[EUR][1000 genomes] |
| rs16844047 | 1.00[EUR][1000 genomes] |
| rs16844059 | 1.00[EUR][1000 genomes] |
| rs16844077 | 1.00[EUR][1000 genomes] |
| rs16856025 | 1.00[EUR][1000 genomes] |
| rs4589693 | 1.00[YRI][hapmap] |
| rs60113359 | 1.00[EUR][1000 genomes] |
| rs72990637 | 1.00[EUR][1000 genomes] |
| rs73964219 | 1.00[EUR][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 | esv2756334 | chr2:141166521-141285622 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | n/a |
| 2 | nsv433205 | chr2:141270270-141285694 | Enhancers | n/a | n/a | inside rSNPs | n/a |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
