Variant report
| Variant | rs268023 |
|---|---|
| Chromosome Location | chr12:45320489-45320490 |
| allele | A/G |
| 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:44)
| rs_ID | r2[population] |
|---|---|
| rs2658991 | 1.00[AMR][1000 genomes] |
| rs268024 | 0.91[YRI][hapmap] |
| rs268025 | 1.00[YRI][hapmap] |
| rs268026 | 1.00[YRI][hapmap] |
| rs268027 | 1.00[YRI][hapmap] |
| rs268028 | 1.00[YRI][hapmap] |
| rs268029 | 0.80[AFR][1000 genomes] |
| rs268033 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs268038 | 0.84[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs2703036 | 1.00[AMR][1000 genomes] |
| rs2703044 | 1.00[AMR][1000 genomes] |
| rs2710427 | 1.00[AMR][1000 genomes] |
| rs2710432 | 1.00[AMR][1000 genomes] |
| rs421642 | 0.91[YRI][hapmap] |
| rs444468 | 0.84[AFR][1000 genomes] |
| rs58109917 | 1.00[AMR][1000 genomes] |
| rs58840891 | 1.00[AMR][1000 genomes] |
| rs73275512 | 1.00[AMR][1000 genomes] |
| rs73275524 | 1.00[AMR][1000 genomes] |
| rs73275531 | 1.00[AMR][1000 genomes] |
| rs73275551 | 1.00[AMR][1000 genomes] |
| rs73275596 | 1.00[AMR][1000 genomes] |
| rs73277300 | 1.00[AMR][1000 genomes] |
| rs73279134 | 1.00[AMR][1000 genomes] |
| rs73279144 | 1.00[AMR][1000 genomes] |
| rs73279145 | 1.00[AMR][1000 genomes] |
| rs73279158 | 1.00[AMR][1000 genomes] |
| rs73279176 | 1.00[AMR][1000 genomes] |
| rs73281008 | 1.00[AMR][1000 genomes] |
| rs73281095 | 1.00[AMR][1000 genomes] |
| rs73281098 | 1.00[AMR][1000 genomes] |
| rs73283039 | 1.00[AMR][1000 genomes] |
| rs73287011 | 1.00[AMR][1000 genomes] |
| rs73288970 | 1.00[AMR][1000 genomes] |
| rs73288973 | 1.00[AMR][1000 genomes] |
| rs73288975 | 1.00[AMR][1000 genomes] |
| rs73288980 | 1.00[AMR][1000 genomes] |
| rs73288988 | 1.00[AMR][1000 genomes] |
| rs73288990 | 1.00[AMR][1000 genomes] |
| rs73288993 | 1.00[AMR][1000 genomes] |
| rs73290682 | 1.00[AMR][1000 genomes] |
| rs73290685 | 1.00[AMR][1000 genomes] |
| rs73290688 | 1.00[AMR][1000 genomes] |
| rs73290690 | 1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv899049 | chr12:45299202-45376053 | Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| 2 | nsv899050 | chr12:45299202-45400614 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| 3 | nsv899051 | chr12:45307633-45376053 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| 4 | nsv527565 | chr12:45319767-45365812 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| 5 | nsv977156 | chr12:45320347-45324286 | Enhancers Weak transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
