Variant report
Variant | rs11755342 |
---|---|
Chromosome Location | chr6:79292666-79292667 |
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] |
---|---|
rs11751885 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11753657 | 0.97[EUR][1000 genomes] |
rs11756326 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs11757555 | 0.83[EUR][1000 genomes] |
rs11759337 | 0.99[EUR][1000 genomes] |
rs16890184 | 0.97[EUR][1000 genomes] |
rs17332393 | 0.99[EUR][1000 genomes] |
rs55644721 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs55858016 | 0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs55883909 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs62426508 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62426531 | 0.84[EUR][1000 genomes] |
rs62426535 | 0.84[EUR][1000 genomes] |
rs62426551 | 0.87[EUR][1000 genomes] |
rs62426552 | 0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs62426553 | 0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62426554 | 0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs9294120 | 0.97[EUR][1000 genomes] |
rs9443600 | 0.93[EUR][1000 genomes] |
rs9443601 | 0.97[EUR][1000 genomes] |
rs9443602 | 0.97[EUR][1000 genomes] |
rs9448490 | 0.99[EUR][1000 genomes] |
rs9448492 | 0.97[EUR][1000 genomes] |
rs9448495 | 0.97[EUR][1000 genomes] |
rs9448498 | 0.97[EUR][1000 genomes] |
rs9448499 | 0.97[EUR][1000 genomes] |
rs9448500 | 0.97[EUR][1000 genomes] |
rs9448505 | 0.94[EUR][1000 genomes] |
rs9448508 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv886235 | chr6:78861808-79369972 | Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv604011 | chr6:79042990-79455282 | Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv886300 | chr6:79129963-79341891 | Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv522646 | chr6:79185106-79333988 | Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1028767 | chr6:79200713-79341224 | Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:79288400-79304400 | Weak transcription | HUVEC | blood vessel |