Variant report
Variant | rs2594123 |
---|---|
Chromosome Location | chr3:60854459-60854460 |
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 |
rs_ID | r2[population] |
---|---|
rs17064044 | 0.85[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap] |
rs17630913 | 0.85[CEU][hapmap];0.81[AMR][1000 genomes] |
rs17630955 | 0.85[CEU][hapmap];1.00[MEX][hapmap];0.81[AMR][1000 genomes] |
rs2594119 | 0.85[CEU][hapmap] |
rs2594130 | 0.83[EUR][1000 genomes] |
rs2594135 | 1.00[CHB][hapmap] |
rs56259187 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs6788545 | 1.00[CHB][hapmap] |
rs717292 | 0.85[CEU][hapmap];0.81[AMR][1000 genomes] |
rs73092711 | 0.81[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs73092730 | 0.83[EUR][1000 genomes] |
rs73097874 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73111756 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534038 | chr3:60781917-60993082 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | esv2757872 | chr3:60781943-61019003 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | esv2759152 | chr3:60781943-61220809 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |