Variant report
Variant | rs35108112 |
---|---|
Chromosome Location | chr15:58608614-58608615 |
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] |
---|---|
rs12683182 | 1.00[ASN][1000 genomes] |
rs12684215 | 1.00[ASN][1000 genomes] |
rs12685903 | 1.00[ASN][1000 genomes] |
rs12686588 | 1.00[ASN][1000 genomes] |
rs1800360 | 0.83[AMR][1000 genomes] |
rs1875835 | 1.00[ASN][1000 genomes] |
rs1886993 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs2121200 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs2404458 | 1.00[ASN][1000 genomes] |
rs3780566 | 1.00[ASN][1000 genomes] |
rs4647348 | 0.89[ASN][1000 genomes] |
rs4647354 | 0.89[ASN][1000 genomes] |
rs4647360 | 1.00[ASN][1000 genomes] |
rs4647367 | 1.00[ASN][1000 genomes] |
rs4647378 | 1.00[ASN][1000 genomes] |
rs4647386 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4647387 | 0.89[ASN][1000 genomes] |
rs4647397 | 1.00[ASN][1000 genomes] |
rs4647398 | 1.00[ASN][1000 genomes] |
rs4647402 | 1.00[ASN][1000 genomes] |
rs4647405 | 1.00[ASN][1000 genomes] |
rs4647408 | 1.00[ASN][1000 genomes] |
rs4647414 | 1.00[ASN][1000 genomes] |
rs4647436 | 1.00[ASN][1000 genomes] |
rs4647437 | 1.00[ASN][1000 genomes] |
rs4647449 | 1.00[ASN][1000 genomes] |
rs4647455 | 0.83[AMR][1000 genomes] |
rs4647465 | 1.00[ASN][1000 genomes] |
rs4647466 | 1.00[ASN][1000 genomes] |
rs4647472 | 1.00[ASN][1000 genomes] |
rs4647473 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4647477 | 1.00[ASN][1000 genomes] |
rs4647484 | 1.00[ASN][1000 genomes] |
rs4647485 | 1.00[ASN][1000 genomes] |
rs4647486 | 1.00[ASN][1000 genomes] |
rs4647491 | 1.00[ASN][1000 genomes] |
rs4647493 | 1.00[ASN][1000 genomes] |
rs4647505 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs4647508 | 1.00[ASN][1000 genomes] |
rs4647509 | 1.00[ASN][1000 genomes] |
rs4647510 | 1.00[ASN][1000 genomes] |
rs4647514 | 1.00[ASN][1000 genomes] |
rs4647516 | 1.00[ASN][1000 genomes] |
rs4647521 | 0.88[ASN][1000 genomes] |
rs57471585 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60228132 | 1.00[ASN][1000 genomes] |
rs7034939 | 0.83[AMR][1000 genomes] |
rs7037729 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73528466 | 0.83[AMR][1000 genomes] |
rs73528478 | 0.83[AMR][1000 genomes] |
rs73530498 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73532103 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73532167 | 0.83[AMR][1000 genomes] |
rs73532195 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73532199 | 0.83[AMR][1000 genomes] |
rs73534887 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73534888 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73534896 | 0.89[ASN][1000 genomes] |
rs73534898 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73537212 | 0.83[AMR][1000 genomes] |
rs73538039 | 0.83[AMR][1000 genomes] |
rs73539203 | 0.83[AMR][1000 genomes] |
rs73541330 | 0.83[AMR][1000 genomes] |
rs7854840 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9792415 | 1.00[ASN][1000 genomes] |
rs9792481 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9792533 | 1.00[ASN][1000 genomes] |
rs9792691 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1047246 | chr15:58375607-58707158 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv833024 | chr15:58447459-58621963 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | nsv1051058 | chr15:58519922-59092530 | Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
4 | nsv542401 | chr15:58519922-59092530 | Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
5 | nsv529717 | chr15:58519923-58756814 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
6 | nsv1042201 | chr15:58520746-58780710 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
7 | nsv569598 | chr15:58552606-58852463 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
8 | nsv904266 | chr15:58580921-58689187 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:58607600-58610600 | Weak transcription | Skeletal Muscle Male | skeletal muscle |