Variant report
| Variant | rs73122578 |
|---|---|
| Chromosome Location | chr3:79359633-79359634 |
| allele | A/C |
| 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:26)
| rs_ID | r2[population] |
|---|---|
| rs12629261 | 0.87[ASN][1000 genomes] |
| rs12629799 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs12638565 | 0.85[ASN][1000 genomes] |
| rs1387668 | 0.89[ASN][1000 genomes] |
| rs17395749 | 0.89[ASN][1000 genomes] |
| rs57012643 | 0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs6782763 | 0.87[ASN][1000 genomes] |
| rs6785230 | 0.87[ASN][1000 genomes] |
| rs6788829 | 0.84[ASN][1000 genomes] |
| rs6788970 | 0.84[ASN][1000 genomes] |
| rs6801558 | 0.84[ASN][1000 genomes] |
| rs73110997 | 0.87[ASN][1000 genomes] |
| rs73112706 | 0.89[ASN][1000 genomes] |
| rs73122554 | 0.89[ASN][1000 genomes] |
| rs73122569 | 0.89[ASN][1000 genomes] |
| rs73122579 | 0.92[ASN][1000 genomes] |
| rs73122586 | 0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
| rs73122590 | 0.89[ASN][1000 genomes] |
| rs73122600 | 0.87[ASN][1000 genomes] |
| rs73125241 | 0.84[ASN][1000 genomes] |
| rs73125242 | 0.84[ASN][1000 genomes] |
| rs73125244 | 0.84[ASN][1000 genomes] |
| rs73125248 | 0.84[ASN][1000 genomes] |
| rs7618575 | 0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs964137 | 0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
| rs9832396 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | esv2763281 | chr3:79246361-79489765 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
| 2 | nsv460727 | chr3:79264611-79406519 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 3 | nsv590736 | chr3:79264611-79406519 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 4 | nsv460730 | chr3:79286801-79411014 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 5 | nsv590737 | chr3:79286801-79411014 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:79356600-79363000 | Weak transcription | Colon Smooth Muscle | Colon |
| 2 | chr3:79358200-79360600 | Weak transcription | Fetal Heart | heart |
