Variant report
| Variant | rs1461372 |
|---|---|
| Chromosome Location | chr11:26394280-26394281 |
| 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:30)
| rs_ID | r2[population] |
|---|---|
| rs1023902 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
| rs10734374 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs1461375 | 1.00[CEU][hapmap] |
| rs1461381 | 1.00[CEU][hapmap] |
| rs1585497 | 1.00[EUR][1000 genomes] |
| rs1841569 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
| rs2045704 | 1.00[CEU][hapmap];0.83[YRI][hapmap] |
| rs2169340 | 1.00[CEU][hapmap] |
| rs2201335 | 0.85[CEU][hapmap] |
| rs2219616 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
| rs4319470 | 1.00[YRI][hapmap] |
| rs4378340 | 0.96[EUR][1000 genomes] |
| rs4500442 | 1.00[CEU][hapmap];0.94[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
| rs4505017 | 0.85[CEU][hapmap] |
| rs55701824 | 0.82[EUR][1000 genomes] |
| rs55740663 | 0.87[EUR][1000 genomes] |
| rs57297880 | 0.87[EUR][1000 genomes] |
| rs57378086 | 0.87[EUR][1000 genomes] |
| rs72876941 | 1.00[EUR][1000 genomes] |
| rs72886219 | 0.87[EUR][1000 genomes] |
| rs72886220 | 0.87[EUR][1000 genomes] |
| rs72886223 | 0.87[EUR][1000 genomes] |
| rs72886227 | 0.87[EUR][1000 genomes] |
| rs72886232 | 0.87[EUR][1000 genomes] |
| rs72886237 | 0.87[EUR][1000 genomes] |
| rs72886263 | 0.87[EUR][1000 genomes] |
| rs72886276 | 0.87[EUR][1000 genomes] |
| rs72886282 | 0.87[EUR][1000 genomes] |
| rs7945236 | 1.00[CEU][hapmap] |
| rs986059 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
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 | esv2422406 | chr11:26329870-26473641 | Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
