Extended Data Fig. 4: Example of a region where a common SNP (in green at chr4:105,236,007) is in close proximity to a TET2 PTV.
From: The burden of rare protein-truncating genetic variants on human lifespan
Example of a region where a common SNP (in green at chr4:105,236,007) is in close proximity to a TET2 PTV. Sequencing reads spanning both variants are consistent with the PTV (the 1-bp deletion at chr4:105,235,982), being somatic in origin.
