Variant report
Variant | rs1437417 |
---|---|
Chromosome Location | chr2:209279587-209279588 |
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 |
rs_ID | r2[population] |
---|---|
rs10186040 | 1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1030879 | 1.00[AMR][1000 genomes] |
rs12624141 | 1.00[AMR][1000 genomes] |
rs1370368 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2028144 | 1.00[AMR][1000 genomes] |
rs2885827 | 1.00[AFR][1000 genomes] |
rs4673400 | 1.00[AMR][1000 genomes] |
rs4675759 | 1.00[AMR][1000 genomes] |
rs6435439 | 1.00[AMR][1000 genomes] |
rs6435447 | 1.00[AMR][1000 genomes] |
rs6710221 | 1.00[AMR][1000 genomes] |
rs6728314 | 1.00[AMR][1000 genomes] |
rs6744236 | 1.00[AMR][1000 genomes] |
rs6744738 | 0.90[AFR][1000 genomes] |
rs7596571 | 1.00[AMR][1000 genomes] |
rs7604977 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs995426 | 1.00[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534496 | chr2:208814372-209302791 | Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
2 | nsv584297 | chr2:209020181-209316760 | Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
No data |