Variant report
Variant | rs10956799 |
---|---|
Chromosome Location | chr8:92283331-92283332 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11990790 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11993280 | 0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11995390 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11995427 | 0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57042938 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73694603 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73694606 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73694607 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73694610 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73694611 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73694622 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028628 | chr8:91680968-92418954 | Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
2 | nsv539672 | chr8:91680968-92418954 | Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
No data |