Multi-modal tissue-aware graph neural network for

Understanding how perturbations influence gene function in a tissue-specific manner is key to uncovering novel drug targets. However, current computational approaches emphasize global network or sequence-derived features over context-driven dependencies. We introduce Mahi, a scalable and interpretable graph neural network framework that learns gene representations by integrating chromatin accessibility, transcription factor binding, histone modifications, and protein structure features in tissue-specific contexts. Through pretraining on tissue-specific network topologies followed by multi-modal feature integration, Mahi learns context-aware gene embeddings across 290 tissues and cell-types. Mahi outperforms sequence-based models in predicting gene essentiality across 1,183 cancer cell lines, demonstrating the advantage of integrating molecular context and functional connectivity. The learned embedding space reveals tissue-specific functional organization, with genes forming distinct clusters reflecting their context-dependent roles.