Variant report
| Variant | rs16841217 |
|---|---|
| Chromosome Location | chr2:209311224-209311225 |
| 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:28)
| rs_ID | r2[population] |
|---|---|
| rs10165447 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
| rs10173178 | 1.00[EUR][1000 genomes] |
| rs11887246 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
| rs11893137 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs11900211 | 1.00[CEU][hapmap];0.87[YRI][hapmap] |
| rs11903831 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
| rs12995209 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12995408 | 1.00[CEU][hapmap] |
| rs13014969 | 1.00[EUR][1000 genomes] |
| rs13015438 | 1.00[AMR][1000 genomes] |
| rs13020468 | 1.00[AMR][1000 genomes] |
| rs13021081 | 1.00[AMR][1000 genomes] |
| rs13034777 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs1370373 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
| rs16840913 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
| rs16841205 | 1.00[CEU][hapmap] |
| rs16841273 | 0.89[EUR][1000 genomes] |
| rs34076187 | 0.89[EUR][1000 genomes] |
| rs34279443 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs34366347 | 1.00[AMR][1000 genomes] |
| rs34757991 | 0.89[EUR][1000 genomes] |
| rs35344600 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6736496 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs71418672 | 1.00[AMR][1000 genomes] |
| rs71418679 | 1.00[AMR][1000 genomes] |
| rs71418693 | 0.89[EUR][1000 genomes] |
| rs73983779 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7578542 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
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 | 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 |
Chromatin state (count:0 , 50 per page) page:
| No data |
