Introducing the EpG2 System: Epigenomic Processes and the Emergent Genome

<b>Background/Objectives:</b> Current genomics research equates the genome with DNA sequence and treats the epigenome as a regulatory layer. This DNA-centric view obscures the fact that genomic identity arises through epigenomic processes. The objective of this article is to reinterpret published findings into a new theoretical framework: the EpG² (Epigenome-Genome) system. <b>Methods:</b> This work develops a new conceptual framework by integrating published evidence from diverse domains-including enhancer biology, overlapping genomic functions, alternative coding frames, zygotic genome activation, and disease-associated loci-and reinterpreting these findings through the lens of epigenomic processes. <b>Results:</b> Evidence shows that enhancers emerge only through the interplay of sequence, transcription factors, and chromatin environment. At fertilization, paternal and maternal genomes remain separate, and a new genome emerges through coordinated epigenomic reprogramming or zygote genome emergence (ZGE). DNA sequence risk variants illustrate the concept of contextual risk alleles, whose effects shift across tissues and developmental stages as epigenomic contexts change. <b>Conclusions:</b> The EpG² system reframes the genome as a processual, emergent entity generated and regulated by epigenomic processes, offering a paradigm for understanding genomic variation beyond DNA sequence.