Variant report
| Variant | rs73435840 |
|---|---|
| Chromosome Location | chr11:23709804-23709805 |
| 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:24)
| rs_ID | r2[population] |
|---|---|
| rs11027431 | 0.86[EUR][1000 genomes] |
| rs11027434 | 1.00[EUR][1000 genomes] |
| rs11027435 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs11027436 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs11027437 | 1.00[EUR][1000 genomes] |
| rs11027438 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs11027440 | 1.00[EUR][1000 genomes] |
| rs11027446 | 0.86[EUR][1000 genomes] |
| rs12269913 | 1.00[EUR][1000 genomes] |
| rs12274900 | 0.97[AFR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12277987 | 0.86[EUR][1000 genomes] |
| rs12280993 | 1.00[EUR][1000 genomes] |
| rs12282955 | 1.00[EUR][1000 genomes] |
| rs12283754 | 1.00[EUR][1000 genomes] |
| rs12288125 | 1.00[EUR][1000 genomes] |
| rs12289552 | 1.00[EUR][1000 genomes] |
| rs12293059 | 0.86[EUR][1000 genomes] |
| rs12293404 | 0.95[AFR][1000 genomes];0.87[AMR][1000 genomes] |
| rs12293501 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs4344483 | 0.83[EUR][1000 genomes] |
| rs58045466 | 1.00[ASN][1000 genomes] |
| rs7108807 | 0.86[EUR][1000 genomes] |
| rs7126806 | 0.86[EUR][1000 genomes] |
| rs73435841 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv553757 | chr11:23564329-23896729 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| 2 | nsv469942 | chr11:23677246-23723766 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
| 3 | nsv897062 | chr11:23687928-24031627 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:23709200-23712800 | Enhancers | Dnd41 | blood |
| 2 | chr11:23709400-23711400 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
