Variant report
| Variant | rs285774 |
|---|---|
| Chromosome Location | chr8:106115255-106115256 |
| allele | G/T |
| 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 | chr8:106110955..106112913-chr8:106113488..106116192,2 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:13)
| rs_ID | r2[population] |
|---|---|
| rs1460586 | 0.94[ASN][1000 genomes] |
| rs16872410 | 0.97[ASN][1000 genomes] |
| rs16872429 | 0.95[ASN][1000 genomes] |
| rs2342458 | 0.97[ASN][1000 genomes] |
| rs28438073 | 0.95[ASN][1000 genomes] |
| rs28558865 | 0.94[ASN][1000 genomes] |
| rs285775 | 0.84[EUR][1000 genomes];0.98[ASN][1000 genomes] |
| rs285776 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes] |
| rs285777 | 0.85[AFR][1000 genomes];0.85[AMR][1000 genomes] |
| rs285799 | 0.84[AMR][1000 genomes] |
| rs6993231 | 0.95[ASN][1000 genomes] |
| rs6993563 | 0.95[ASN][1000 genomes] |
| rs7819593 | 0.97[ASN][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 | esv2762763 | chr8:105943295-106218634 | Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| 2 | nsv891253 | chr8:105994885-106251476 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| 3 | nsv891254 | chr8:106060970-106175867 | Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| 4 | nsv465755 | chr8:106107997-106121745 | Weak transcription Enhancers Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | n/a |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:106113600-106118800 | Weak transcription | HUVEC | blood vessel |
