Variant report
| Variant | rs16831286 |
|---|---|
| Chromosome Location | chr3:160323722-160323723 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr3:160283211..160285094-chr3:160322353..160324060,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000229320 | Chromatin interaction |
| ENSG00000186432 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:18)
| rs_ID | r2[population] |
|---|---|
| rs10212356 | 1.00[CEU][hapmap];0.93[EUR][1000 genomes] |
| rs11919703 | 0.80[EUR][1000 genomes] |
| rs13314803 | 0.80[EUR][1000 genomes] |
| rs16831313 | 0.94[EUR][1000 genomes] |
| rs1920661 | 1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.93[EUR][1000 genomes] |
| rs2178454 | 0.94[EUR][1000 genomes] |
| rs28631610 | 0.93[EUR][1000 genomes] |
| rs55804574 | 0.94[EUR][1000 genomes] |
| rs6441326 | 0.94[EUR][1000 genomes] |
| rs6778401 | 1.00[EUR][1000 genomes] |
| rs6778711 | 1.00[EUR][1000 genomes] |
| rs9813697 | 1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap] |
| rs9825299 | 0.93[EUR][1000 genomes] |
| rs9829578 | 0.80[EUR][1000 genomes] |
| rs9838380 | 0.94[EUR][1000 genomes] |
| rs9847211 | 0.88[EUR][1000 genomes] |
| rs9857038 | 0.94[EUR][1000 genomes] |
| rs9857327 | 0.93[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv532666 | chr3:159777847-160703202 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 271 gene(s) | inside rSNPs | diseases |
| 2 | nsv1000453 | chr3:159853305-160366357 | Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 259 gene(s) | inside rSNPs | diseases |
| 3 | nsv536779 | chr3:159853305-160366357 | Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 259 gene(s) | inside rSNPs | diseases |
| 4 | nsv4089 | chr3:160284848-160330024 | Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
