Variant report
Variant | rs56176715 |
---|---|
Chromosome Location | chr6:100765660-100765661 |
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] |
---|---|
rs11962725 | 1.00[AMR][1000 genomes] |
rs11964322 | 0.80[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55692601 | 1.00[AMR][1000 genomes] |
rs56876848 | 1.00[AMR][1000 genomes] |
rs57335321 | 1.00[AMR][1000 genomes] |
rs59301700 | 1.00[AMR][1000 genomes] |
rs60973981 | 1.00[AMR][1000 genomes] |
rs73760809 | 1.00[AMR][1000 genomes] |
rs73760820 | 1.00[AMR][1000 genomes] |
rs73760821 | 1.00[AMR][1000 genomes] |
rs73760822 | 1.00[AMR][1000 genomes] |
rs73760824 | 1.00[AMR][1000 genomes] |
rs73760825 | 1.00[AMR][1000 genomes] |
rs73760826 | 1.00[AMR][1000 genomes] |
rs73760828 | 1.00[AMR][1000 genomes] |
rs73760831 | 1.00[AMR][1000 genomes] |
rs73760853 | 1.00[AMR][1000 genomes] |
rs73760862 | 1.00[AMR][1000 genomes] |
rs73760864 | 1.00[AMR][1000 genomes] |
rs73760865 | 1.00[AMR][1000 genomes] |
rs73760866 | 1.00[AMR][1000 genomes] |
rs73760870 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949535 | chr6:100740293-101469052 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:100760600-100766000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |