The structure of eukaryotic origins is a long-standing question in the DNA replication field, and the universal features that define the genomic regions acting as replication starting sites remain unclear. In this study, we employed the stranded SNS-seq methodology, a high-throughput sequencing method that preserves the directionality of short nascent strands, to map a set of origins in Trypanosoma brucei. This approach enhanced the specificity and resolution of origin mapping. Our findings indicated that replication predominantly initiates in intergenic regions, situated between poly(dA) and poly(dT) enriched sequences. Experimentally detected G4 structures were observed in the vicinity of some origins. These structures were observed to be embedded within poly(dA) enriched sequences in a strand-specific manner, with the G4s on the plus strand located upstream and the G4s on the minus strand located downstream of the centre. The centre of origin was mainly characterised by low nucleosome occupancy, with flanking regions displaying high nucleosome occupancy. Additionally, our findings revealed that 90% of origins overlapped with previously reported R-loops. To gain further insight, DNA combing analysis was employed to compare replication at the single-cell level with that observed at the entire cell population level. Finally, a model of eukaryotic origin has been proposed.