Variant report
Variant | rs7318981 |
---|---|
Chromosome Location | chr13:65611468-65611469 |
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] |
---|---|
rs1113141 | 0.83[ASN][1000 genomes] |
rs1340812 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1890283 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2137512 | 0.83[ASN][1000 genomes] |
rs4144449 | 0.90[ASN][1000 genomes] |
rs4453355 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4883744 | 0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs61953880 | 0.83[EUR][1000 genomes] |
rs61953883 | 0.87[EUR][1000 genomes] |
rs6562380 | 0.83[ASN][1000 genomes] |
rs6562381 | 0.83[ASN][1000 genomes] |
rs7319969 | 0.87[EUR][1000 genomes] |
rs7324694 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7329489 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7330513 | 0.83[ASN][1000 genomes] |
rs7335620 | 0.83[ASN][1000 genomes] |
rs7981527 | 0.81[EUR][1000 genomes] |
rs7984878 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7985378 | 0.87[ASN][1000 genomes] |
rs7998849 | 0.83[ASN][1000 genomes] |
rs9317458 | 0.83[ASN][1000 genomes] |
rs9317462 | 1.00[CEU][hapmap];1.00[JPT][hapmap] |
rs9317463 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs9528849 | 0.83[ASN][1000 genomes] |
rs9528876 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9528889 | 0.95[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs9540266 | 0.82[EUR][1000 genomes] |
rs9540269 | 0.87[EUR][1000 genomes] |
rs9540270 | 0.87[EUR][1000 genomes] |
rs9540271 | 0.87[EUR][1000 genomes] |
rs9540298 | 0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9540319 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs9540330 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9571306 | 0.83[ASN][1000 genomes] |
rs9598859 | 0.83[ASN][1000 genomes] |
rs9598861 | 0.85[EUR][1000 genomes] |
rs9598878 | 0.82[EUR][1000 genomes] |
rs9598879 | 0.87[EUR][1000 genomes] |
rs9598880 | 0.87[EUR][1000 genomes] |
rs9598892 | 1.00[CEU][hapmap] |
rs9598940 | 0.93[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9598945 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs986812 | 0.83[ASN][1000 genomes] |
rs986813 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1045954 | chr13:65495013-65842827 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1046706 | chr13:65495013-66210226 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv541809 | chr13:65495013-66210226 | Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv900373 | chr13:65495897-65775294 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv915632 | chr13:65531495-65834877 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
6 | nsv1037329 | chr13:65583733-65673656 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:65611200-65611600 | Enhancers | A549 | lung |