Variant report
Variant | rs781279 |
---|---|
Chromosome Location | chr2:189658699-189658700 |
allele | G/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] |
---|---|
rs10497682 | 0.97[EUR][1000 genomes] |
rs1084170 | 0.87[EUR][1000 genomes] |
rs11901190 | 0.97[EUR][1000 genomes] |
rs16830514 | 0.84[EUR][1000 genomes] |
rs16830657 | 0.97[EUR][1000 genomes] |
rs2690759 | 0.84[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs2690761 | 0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2708196 | 0.84[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs2708198 | 0.84[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs2708200 | 0.84[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs58547931 | 0.93[EUR][1000 genomes] |
rs6745069 | 0.97[EUR][1000 genomes] |
rs6745091 | 0.97[EUR][1000 genomes] |
rs781236 | 0.97[EUR][1000 genomes] |
rs781237 | 0.84[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs781248 | 0.84[EUR][1000 genomes] |
rs781253 | 0.84[EUR][1000 genomes] |
rs781261 | 0.90[AFR][1000 genomes] |
rs781263 | 0.97[EUR][1000 genomes] |
rs781280 | 0.93[AMR][1000 genomes] |
rs781281 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs781283 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs781284 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs781285 | 0.86[AMR][1000 genomes] |
rs781286 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs781287 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs781288 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs940461 | 0.97[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1003974 | chr2:189331760-189827814 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
2 | nsv1000932 | chr2:189542210-189677277 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv536088 | chr2:189542210-189677277 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv875606 | chr2:189579045-189688463 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv875607 | chr2:189579045-189711790 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1008847 | chr2:189603961-189769705 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv997454 | chr2:189615728-189770133 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | nsv1002175 | chr2:189615728-189776301 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:189654800-189661400 | Weak transcription | NHLF | lung |
2 | chr2:189655200-189662000 | Weak transcription | Fetal Lung | lung |
3 | chr2:189655800-189660800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |