Variant report
Variant | rs12156117 |
---|---|
Chromosome Location | chr8:10947050-10947051 |
allele | C/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] |
---|---|
rs10087767 | 1.00[ASN][1000 genomes] |
rs11783227 | 1.00[ASN][1000 genomes] |
rs11785392 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13248264 | 0.85[AMR][1000 genomes] |
rs13248300 | 0.83[EUR][1000 genomes] |
rs13265533 | 0.84[EUR][1000 genomes] |
rs13273857 | 1.00[ASN][1000 genomes] |
rs13275102 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13276836 | 1.00[ASN][1000 genomes] |
rs17152841 | 0.89[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs17779791 | 0.83[EUR][1000 genomes] |
rs2409692 | 0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2409693 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2409695 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36089015 | 1.00[ASN][1000 genomes] |
rs4618656 | 1.00[ASN][1000 genomes] |
rs4840536 | 0.81[AMR][1000 genomes] |
rs4840541 | 0.87[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4841491 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs4841508 | 1.00[ASN][1000 genomes] |
rs67841554 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7000132 | 1.00[ASN][1000 genomes] |
rs7823610 | 0.80[EUR][1000 genomes] |
rs9657544 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9657545 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1035072 | chr8:10819444-11480692 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
2 | nsv539473 | chr8:10819444-11480692 | Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
3 | esv1815171 | chr8:10940039-11128712 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
4 | nsv1025426 | chr8:10942929-11037903 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:10943000-10948400 | Weak transcription | Gastric | stomach |