Groundbreaking research introduces the EPI-Clone method to trace blood cell clones and understand blood aging dynamics at the cellular level.EPI-Clone utilizes a targeted methylation panel focusing on 448 CpG sites to capture heritable somatic epigenetic changes in DNA methylation patterns.The method was applied to human bone marrow samples from donors of various ages, revealing insights into genetic mutations and epigenetic states.Using a statistical framework called CHOIR, the study identified expanded clones by combining epigenetic signatures and surface marker expression.Epigenetic marks proved reliable for identifying genetic clonal identity, aligning well with known clonal hematopoiesis clones.The EPI-Clone method detected canonical clonal hematopoiesis mutations and revealed additional clonal expansions in the cohort.Analysis extended to different immune cell types, showing distinct clonal segregation and ontogenetic trajectories within hematopoiesis.EPI-Clone's sensitivity identified small CH clones and revealed diversification within large clones, offering insights into clonal evolution.The study underscores EPI-Clone's ability to map hematopoietic clonal expansions, providing detailed insights into blood aging and clonal dynamics.Integration of epigenetic and phenotypic data with mutation analyses opens avenues for understanding clonal hematopoiesis in age-related diseases.