White matter (WM) functional activity has been reliably detected through functional magnetic resonance imaging (fMRI). Previous studies have primarily examined WM bundles as unified entities, thereby obscuring the functional heterogeneity inherent within these bundles. Here, for the first time, we investigate the function of sub‐bundles of a prototypical visual WM tract—the optic radiation (OR). We use the 7T retinotopy dataset from the Human Connectome Project (HCP) to reconstruct OR and further subdivide the OR into sub‐bundles based on the fiber's termination in the primary visual cortex (V1). The population receptive field (pRF) model is then applied to evaluate the retinotopic properties of these sub‐bundles, and the consistency of the pRF properties of sub‐bundles with those of V1 subfields is evaluated. Furthermore, we utilize the HCP working memory dataset to evaluate the activations of the foveal and peripheral OR sub‐bundles, along with LGN and V1 subfields, during 0‐back and 2‐back tasks. We then evaluate differences in 2bk‐0bk contrast between foveal and peripheral sub‐bundles (or subfields), and further examine potential relationships between 2bk‐0bk contrast and 2‐back task d‐prime. The results show that the pRF properties of OR sub‐bundles exhibit standard retinotopic properties and are typically similar to the properties of V1 subfields. Notably, activations during the 2‐back task consistently surpass those under the 0‐back task across foveal and peripheral OR sub‐bundles, as well as LGN and V1 subfields. The foveal V1 displays significantly higher 2bk‐0bk contrast than peripheral V1. The 2‐back task d‐prime shows strong correlations with 2bk‐0bk contrast for foveal and peripheral OR fibers. These findings demonstrate that the blood oxygen level‐dependent (BOLD) signals of OR sub‐bundles encode high‐fidelity visual information, underscoring the feasibility of assessing WM functional activity at the sub‐bundle level. Additionally, the study highlights the role of OR in the top‐down processes of visual working memory beyond the bottom‐up processes for visual information transmission. Conclusively, this study innovatively proposes a novel paradigm for analyzing WM fiber tracts at the individual sub‐bundle level and expands understanding of OR function.