Variant report
Variant | rs73012606 |
---|---|
Chromosome Location | chr3:143631527-143631528 |
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] |
---|---|
rs11917171 | 1.00[AMR][1000 genomes] |
rs11921390 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11928979 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55868484 | 1.00[AMR][1000 genomes] |
rs56865417 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57368166 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60336255 | 1.00[AMR][1000 genomes] |
rs60513603 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60542095 | 1.00[AMR][1000 genomes] |
rs60777016 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60831305 | 1.00[AMR][1000 genomes] |
rs6771320 | 1.00[AMR][1000 genomes] |
rs6794428 | 1.00[AMR][1000 genomes] |
rs72995499 | 1.00[AMR][1000 genomes] |
rs72997303 | 1.00[AMR][1000 genomes] |
rs72997304 | 1.00[AMR][1000 genomes] |
rs73002692 | 1.00[AMR][1000 genomes] |
rs73010561 | 1.00[AMR][1000 genomes] |
rs73010568 | 1.00[AMR][1000 genomes] |
rs73010581 | 1.00[AMR][1000 genomes] |
rs73010585 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73010586 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7615162 | 1.00[AMR][1000 genomes] |
rs7615541 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877568 | chr3:143621140-143992630 | Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:143629800-143640400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |