Variant report
| Variant | rs2450464 |
|---|---|
| Chromosome Location | chr10:61691728-61691729 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:2 , 50 per page) page:
1
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000108091 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:13)
| rs_ID | r2[population] |
|---|---|
| rs1171833 | 0.84[EUR][1000 genomes] |
| rs1183347 | 0.84[EUR][1000 genomes] |
| rs1664276 | 0.87[EUR][1000 genomes] |
| rs1664278 | 0.86[EUR][1000 genomes] |
| rs1664279 | 0.86[EUR][1000 genomes] |
| rs1664280 | 0.86[EUR][1000 genomes] |
| rs1664281 | 0.86[EUR][1000 genomes] |
| rs1684904 | 0.86[EUR][1000 genomes] |
| rs1684916 | 0.86[EUR][1000 genomes] |
| rs2440916 | 0.87[EUR][1000 genomes] |
| rs2440918 | 0.86[EUR][1000 genomes] |
| rs2450462 | 0.86[EUR][1000 genomes] |
| rs2450463 | 0.86[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 | esv1800316 | chr10:61639599-61700473 | Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 8 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
