Variant report
Variant | rs4586911 |
---|---|
Chromosome Location | chr4:120752385-120752386 |
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] |
---|---|
rs10013306 | 1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs10452196 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs10518339 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs16997607 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17006835 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17006879 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17006974 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs58946926 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6836195 | 0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6845298 | 0.89[EUR][1000 genomes] |
rs6852136 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6855466 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72910441 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72910468 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72910474 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72910481 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72910484 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72910490 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72910492 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs9307481 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9993750 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916641 | chr4:119780023-120777320 | Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 72 gene(s) | inside rSNPs | diseases |
2 | nsv532739 | chr4:120392824-121098103 | Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
3 | esv3443538 | chr4:120725398-120755486 | Weak transcription Enhancers | TF binding regionCpG islandlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:120751000-120753800 | Weak transcription | Aorta | Aorta |