Variant report
| Variant | rs728124 |
|---|---|
| Chromosome Location | chr14:78842275-78842276 |
| allele | C/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:36)
| rs_ID | r2[population] |
|---|---|
| rs10135111 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs10135475 | 1.00[AMR][1000 genomes] |
| rs11159360 | 1.00[AMR][1000 genomes] |
| rs1156946 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs1990530 | 1.00[AMR][1000 genomes] |
| rs2052202 | 1.00[AMR][1000 genomes] |
| rs2052203 | 1.00[AMR][1000 genomes] |
| rs2110424 | 1.00[AMR][1000 genomes] |
| rs2192413 | 1.00[AMR][1000 genomes] |
| rs2192414 | 1.00[AMR][1000 genomes] |
| rs2192415 | 1.00[AMR][1000 genomes] |
| rs2192421 | 1.00[AMR][1000 genomes] |
| rs2215830 | 1.00[AMR][1000 genomes] |
| rs2215831 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs2215832 | 1.00[AMR][1000 genomes] |
| rs2215833 | 1.00[AMR][1000 genomes] |
| rs2366099 | 1.00[AMR][1000 genomes] |
| rs2366156 | 1.00[AMR][1000 genomes] |
| rs2886581 | 1.00[AMR][1000 genomes] |
| rs4899709 | 1.00[AMR][1000 genomes] |
| rs4899710 | 1.00[AMR][1000 genomes] |
| rs4903756 | 1.00[AMR][1000 genomes] |
| rs4903765 | 1.00[AMR][1000 genomes] |
| rs6574444 | 1.00[AMR][1000 genomes] |
| rs6574449 | 1.00[AMR][1000 genomes] |
| rs6574450 | 1.00[AMR][1000 genomes] |
| rs7157498 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs7158579 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs7159492 | 1.00[AMR][1000 genomes] |
| rs8003367 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs8003391 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs8005882 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs8008949 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs8017182 | 1.00[AMR][1000 genomes] |
| rs8020588 | 1.00[YRI][hapmap] |
| rs8020682 | 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 | nsv832837 | chr14:78766805-78946526 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
