Variant report
| Variant | rs7997711 |
|---|---|
| Chromosome Location | chr13:76704789-76704790 |
| 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] |
|---|---|
| rs17065542 | 0.95[AMR][1000 genomes];0.87[EUR][1000 genomes] |
| rs4052613 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs4242962 | 1.00[CEU][hapmap];0.80[EUR][1000 genomes] |
| rs55780287 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs56198072 | 0.95[AMR][1000 genomes];0.80[EUR][1000 genomes] |
| rs57076889 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs60058668 | 1.00[EUR][1000 genomes] |
| rs73215669 | 0.80[EUR][1000 genomes] |
| rs73215673 | 0.80[EUR][1000 genomes] |
| rs73215675 | 1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
| rs73215686 | 0.95[AMR][1000 genomes];0.80[EUR][1000 genomes] |
| rs73215696 | 0.80[EUR][1000 genomes] |
| rs73215697 | 0.80[EUR][1000 genomes] |
| rs73217726 | 0.90[AMR][1000 genomes];0.87[EUR][1000 genomes] |
| rs73219844 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73219846 | 1.00[EUR][1000 genomes] |
| rs73219851 | 1.00[EUR][1000 genomes] |
| rs73219852 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73224121 | 1.00[EUR][1000 genomes] |
| rs73224127 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73224133 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73224154 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7985909 | 0.87[EUR][1000 genomes] |
| rs7990742 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
| rs7990852 | 0.86[AMR][1000 genomes] |
| rs7990902 | 1.00[AMR][1000 genomes] |
| rs7994458 | 1.00[CEU][hapmap];0.80[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1054431 | chr13:76460431-76885094 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| 2 | nsv541837 | chr13:76460431-76885094 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| 3 | nsv900580 | chr13:76665408-76735400 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:76704000-76705800 | Weak transcription | Fetal Heart | heart |
| 2 | chr13:76704000-76705800 | Weak transcription | Fetal Lung | lung |
