Variant report
| Variant | rs436000 |
|---|---|
| Chromosome Location | chr2:76240361-76240362 |
| allele | A/C |
| 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:39)
| rs_ID | r2[population] |
|---|---|
| rs10195421 | 0.81[CHB][hapmap] |
| rs11126493 | 0.83[AFR][1000 genomes] |
| rs12612816 | 0.81[ASN][1000 genomes] |
| rs1524215 | 0.94[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap] |
| rs317234 | 0.97[EUR][1000 genomes];0.84[ASN][1000 genomes] |
| rs317235 | 0.85[AFR][1000 genomes] |
| rs317236 | 0.81[AFR][1000 genomes] |
| rs317242 | 0.80[AFR][1000 genomes] |
| rs365027 | 0.82[ASN][1000 genomes] |
| rs367949 | 0.95[AFR][1000 genomes];0.85[ASN][1000 genomes] |
| rs371016 | 0.81[ASN][1000 genomes] |
| rs375530 | 0.81[ASN][1000 genomes] |
| rs379732 | 0.91[AFR][1000 genomes];0.86[ASN][1000 genomes] |
| rs380810 | 0.81[ASN][1000 genomes] |
| rs381100 | 0.97[EUR][1000 genomes];0.84[ASN][1000 genomes] |
| rs384304 | 0.81[ASN][1000 genomes] |
| rs3843860 | 0.83[AFR][1000 genomes] |
| rs3843861 | 0.81[AFR][1000 genomes] |
| rs3849395 | 0.83[AFR][1000 genomes] |
| rs3849396 | 0.81[AFR][1000 genomes] |
| rs389616 | 0.81[ASN][1000 genomes] |
| rs390189 | 0.81[ASN][1000 genomes] |
| rs390652 | 0.81[ASN][1000 genomes] |
| rs390687 | 0.81[ASN][1000 genomes] |
| rs3910651 | 0.83[AFR][1000 genomes] |
| rs394278 | 0.81[ASN][1000 genomes] |
| rs397424 | 0.81[ASN][1000 genomes] |
| rs403631 | 0.81[ASN][1000 genomes] |
| rs410367 | 0.81[ASN][1000 genomes] |
| rs410954 | 0.81[ASN][1000 genomes] |
| rs416093 | 0.81[ASN][1000 genomes] |
| rs416264 | 0.81[ASN][1000 genomes] |
| rs421884 | 0.81[ASN][1000 genomes] |
| rs422600 | 0.81[ASN][1000 genomes] |
| rs432117 | 0.81[ASN][1000 genomes] |
| rs441584 | 0.86[AFR][1000 genomes] |
| rs450596 | 0.97[EUR][1000 genomes];0.85[ASN][1000 genomes] |
| rs454793 | 0.81[ASN][1000 genomes] |
| rs4853190 | 0.81[AFR][1000 genomes] |
Variant related diseases (count:1)
| Disease | PMID | Source |
|---|---|---|
| Economic and political preferences (fairness) | 22566634 | GWAS catalog |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:76237600-76243600 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
