Variant report
Variant | rs7926834 |
---|---|
Chromosome Location | chr11:84796795-84796796 |
allele | A/C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs11819885 | 1.00[EUR][1000 genomes] |
rs11820110 | 1.00[EUR][1000 genomes] |
rs11821196 | 1.00[AMR][1000 genomes] |
rs11821930 | 1.00[EUR][1000 genomes] |
rs11822005 | 1.00[EUR][1000 genomes] |
rs11822075 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11822292 | 1.00[AMR][1000 genomes] |
rs11823066 | 1.00[EUR][1000 genomes] |
rs11823863 | 1.00[EUR][1000 genomes] |
rs11823950 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11824142 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11825118 | 1.00[EUR][1000 genomes] |
rs11825860 | 1.00[AMR][1000 genomes] |
rs11827460 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11828495 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11828752 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11829016 | 0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55649137 | 1.00[EUR][1000 genomes] |
rs55893782 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55966246 | 1.00[AMR][1000 genomes] |
rs57010664 | 1.00[EUR][1000 genomes] |
rs57374267 | 1.00[EUR][1000 genomes] |
rs57513498 | 1.00[EUR][1000 genomes] |
rs57811920 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58434167 | 0.80[AFR][1000 genomes] |
rs58960201 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59019401 | 1.00[EUR][1000 genomes] |
rs59597223 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59601533 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60734054 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7113785 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948410 | chr11:83918339-84812001 | Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv430415 | chr11:84661652-84833852 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1055097 | chr11:84672444-84810441 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1040393 | chr11:84708402-84866594 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv527535 | chr11:84724795-84895033 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | nsv528491 | chr11:84724795-84895033 | Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
7 | nsv1044370 | chr11:84748993-85293233 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:84794400-84798400 | Weak transcription | Aorta | Aorta |