Variant report
| Variant | rs2698334 |
|---|---|
| Chromosome Location | chr3:111137691-111137692 |
| allele | G/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:20)
| rs_ID | r2[population] |
|---|---|
| rs12695238 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs12695239 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs1489037 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs1529055 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs1529061 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs1529064 | 1.00[EUR][1000 genomes] |
| rs1586561 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs2634536 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2646970 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2646991 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs2646992 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs2698335 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2698336 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2932043 | 0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2950985 | 1.00[EUR][1000 genomes] |
| rs2958073 | 0.90[AMR][1000 genomes] |
| rs4682040 | 1.00[EUR][1000 genomes] |
| rs4682041 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs72946117 | 1.00[EUR][1000 genomes] |
| rs973209 | 1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv460821 | chr3:110637471-111501097 | Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
| 2 | nsv591275 | chr3:110637471-111501097 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:111137000-111137800 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
