Variant report
Variant | rs73094499 |
---|---|
Chromosome Location | chr12:39925654-39925655 |
allele | A/G |
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] |
---|---|
rs1567738 | 1.00[AMR][1000 genomes] |
rs73086879 | 1.00[AMR][1000 genomes] |
rs73086887 | 1.00[AMR][1000 genomes] |
rs73086888 | 1.00[AMR][1000 genomes] |
rs73086895 | 1.00[AMR][1000 genomes] |
rs73086896 | 1.00[AMR][1000 genomes] |
rs73088803 | 1.00[AMR][1000 genomes] |
rs73088804 | 1.00[AMR][1000 genomes] |
rs73088806 | 1.00[AMR][1000 genomes] |
rs73088808 | 1.00[AMR][1000 genomes] |
rs73088811 | 1.00[AMR][1000 genomes] |
rs73088812 | 1.00[AMR][1000 genomes] |
rs73094416 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094426 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094430 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094441 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094443 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094451 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094465 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094466 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094469 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094480 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094482 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094497 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094498 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094502 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73096503 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73096504 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73096507 | 1.00[AMR][1000 genomes] |
rs73096509 | 1.00[AMR][1000 genomes] |
rs73096513 | 1.00[AMR][1000 genomes] |
rs73096521 | 1.00[AMR][1000 genomes] |
rs73096524 | 1.00[AMR][1000 genomes] |
rs73096528 | 1.00[AMR][1000 genomes] |
rs73096539 | 1.00[AMR][1000 genomes] |
rs73096542 | 1.00[AMR][1000 genomes] |
rs73096551 | 1.00[AMR][1000 genomes] |
rs73096571 | 1.00[AMR][1000 genomes] |
rs73096578 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531527 | chr12:39680812-40182822 | Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
2 | nsv1048933 | chr12:39886665-39946270 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv1037457 | chr12:39898349-40245401 | Weak transcription Enhancers Strong transcription 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 | 9 gene(s) | inside rSNPs | diseases |
4 | nsv541480 | chr12:39898349-40245401 | Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
5 | nsv1039645 | chr12:39903123-40022029 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:39925400-39925800 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |