Variant report
Variant | rs55955516 |
---|---|
Chromosome Location | chr4:130042816-130042817 |
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 |
rs_ID | r2[population] |
---|---|
rs55707740 | 1.00[AFR][1000 genomes] |
rs55714747 | 1.00[AFR][1000 genomes] |
rs55764329 | 0.91[AFR][1000 genomes] |
rs56002856 | 1.00[AFR][1000 genomes] |
rs56069250 | 1.00[AFR][1000 genomes] |
rs56721576 | 1.00[AFR][1000 genomes] |
rs57243721 | 0.83[AFR][1000 genomes] |
rs57542268 | 1.00[AFR][1000 genomes] |
rs57869637 | 1.00[AMR][1000 genomes] |
rs58053026 | 0.91[AFR][1000 genomes] |
rs58701517 | 1.00[AFR][1000 genomes] |
rs60005322 | 1.00[AFR][1000 genomes] |
rs60064190 | 1.00[AMR][1000 genomes] |
rs60227965 | 0.83[AFR][1000 genomes] |
rs61267810 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs61700015 | 1.00[AFR][1000 genomes] |
rs73847304 | 0.91[AFR][1000 genomes] |
rs73847305 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73847307 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73847310 | 0.91[AFR][1000 genomes] |
rs73847314 | 0.91[AFR][1000 genomes] |
rs73847316 | 1.00[AFR][1000 genomes] |
rs73847317 | 1.00[AFR][1000 genomes] |
rs73847322 | 1.00[AFR][1000 genomes] |
rs73847323 | 1.00[AFR][1000 genomes] |
rs73847326 | 1.00[AFR][1000 genomes] |
rs73847327 | 1.00[AFR][1000 genomes] |
rs73847329 | 1.00[AFR][1000 genomes] |
rs73847331 | 1.00[AFR][1000 genomes] |
rs73847332 | 1.00[AFR][1000 genomes] |
rs73847333 | 1.00[AFR][1000 genomes] |
rs73847334 | 1.00[AFR][1000 genomes] |
rs73847341 | 1.00[AFR][1000 genomes] |
rs73847342 | 1.00[AFR][1000 genomes] |
rs73847345 | 1.00[AFR][1000 genomes] |
rs73847347 | 1.00[AFR][1000 genomes] |
rs73847354 | 1.00[AFR][1000 genomes] |
rs73847355 | 1.00[AFR][1000 genomes] |
rs73847356 | 0.91[AFR][1000 genomes] |
rs73847358 | 1.00[AFR][1000 genomes] |
rs73847375 | 1.00[AFR][1000 genomes] |
rs73847378 | 1.00[AFR][1000 genomes] |
rs73847380 | 1.00[AFR][1000 genomes] |
rs73847383 | 0.83[AFR][1000 genomes] |
rs73847391 | 0.83[AFR][1000 genomes] |
rs73847392 | 1.00[AFR][1000 genomes] |
rs73847395 | 0.83[AFR][1000 genomes] |
rs73847398 | 0.83[AFR][1000 genomes] |
rs73847399 | 0.83[AFR][1000 genomes] |
rs73848906 | 0.91[AFR][1000 genomes] |
rs73848910 | 1.00[AFR][1000 genomes] |
rs73848913 | 1.00[AFR][1000 genomes] |
rs73848917 | 1.00[AMR][1000 genomes] |
rs73848934 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73848943 | 1.00[AMR][1000 genomes] |
rs73848945 | 1.00[AMR][1000 genomes] |
rs73848949 | 1.00[AMR][1000 genomes] |
rs73850035 | 1.00[AFR][1000 genomes] |
rs73850039 | 1.00[AFR][1000 genomes] |
rs73850061 | 1.00[AFR][1000 genomes] |
rs73850062 | 0.91[AFR][1000 genomes] |
rs73850063 | 0.91[AFR][1000 genomes] |
rs73850064 | 0.91[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869258 | chr4:129191619-130138148 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 79 gene(s) | inside rSNPs | diseases |
2 | nsv534538 | chr4:129799138-130431688 | Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv879931 | chr4:129939775-130178102 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:130032400-130052200 | Weak transcription | Aorta | Aorta |
2 | chr4:130036000-130044600 | Weak transcription | Pancreas | Pancrea |