Variant report
Variant | rs7265005 |
---|---|
Chromosome Location | chr20:10807831-10807832 |
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] |
---|---|
rs16991987 | 1.00[AMR][1000 genomes] |
rs56348465 | 1.00[AMR][1000 genomes] |
rs58036995 | 1.00[AMR][1000 genomes] |
rs58565167 | 1.00[AMR][1000 genomes] |
rs6032968 | 1.00[AMR][1000 genomes] |
rs6040190 | 1.00[AMR][1000 genomes] |
rs6040193 | 1.00[AMR][1000 genomes] |
rs7261930 | 1.00[AMR][1000 genomes] |
rs7274741 | 1.00[AMR][1000 genomes] |
rs73896403 | 1.00[AMR][1000 genomes] |
rs73898834 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73898836 | 1.00[AMR][1000 genomes] |
rs73898841 | 1.00[AMR][1000 genomes] |
rs73898847 | 0.86[AFR][1000 genomes] |
rs73898852 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73898854 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73898858 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73898860 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73898863 | 1.00[AMR][1000 genomes] |
rs73898864 | 1.00[AMR][1000 genomes] |
rs73898866 | 1.00[AMR][1000 genomes] |
rs73898870 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv522874 | chr20:9899439-10819210 | Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 57 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:10799600-10812600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |