Variant report
| Variant | rs72735390 |
|---|---|
| Chromosome Location | chr9:93440238-93440239 |
| 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:27)
| rs_ID | r2[population] |
|---|---|
| rs1542479 | 0.83[ASN][1000 genomes] |
| rs16906728 | 0.90[ASN][1000 genomes] |
| rs2297353 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2297354 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs72733262 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs72735386 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs72735388 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs72735391 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs72735392 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs72735395 | 0.87[ASN][1000 genomes] |
| rs72744799 | 0.86[ASN][1000 genomes] |
| rs72744801 | 0.86[ASN][1000 genomes] |
| rs72746503 | 0.86[ASN][1000 genomes] |
| rs72746505 | 0.86[ASN][1000 genomes] |
| rs72746506 | 0.81[ASN][1000 genomes] |
| rs72746508 | 0.86[ASN][1000 genomes] |
| rs72746510 | 0.86[ASN][1000 genomes] |
| rs72757615 | 0.86[ASN][1000 genomes] |
| rs72757616 | 0.86[ASN][1000 genomes] |
| rs72757617 | 0.86[ASN][1000 genomes] |
| rs72757620 | 0.86[ASN][1000 genomes] |
| rs72757623 | 0.88[ASN][1000 genomes] |
| rs72757626 | 0.94[ASN][1000 genomes] |
| rs72757629 | 0.94[ASN][1000 genomes] |
| rs72757630 | 0.94[ASN][1000 genomes] |
| rs72757631 | 0.94[ASN][1000 genomes] |
| rs72757639 | 0.92[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 | nsv1041278 | chr9:92965701-93560454 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
| 2 | nsv1046989 | chr9:93353987-93800416 | Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
| 3 | nsv482757 | chr9:93356095-93543903 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
| 4 | nsv6610 | chr9:93428408-93473346 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:93439800-93440600 | Enhancers | Primary neutrophils fromperipheralblood | blood |
