Fig. 3From: Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populationsFunctional annotation of putatively Polynesian enriched variants identified by mid-pass sequencing. Variants are characterized as being absent (orange) or rare (MAF < 1%, green) in 1000 Genomes Phase 3 and common (MAF > 5%) in the study dataset. Breakdown of variants as a function of type (SNV/INDEL, A), class (coding, regulatory, or other, B), and predicted effect (C). Indels located in high-confidence regions of the genome and all SNVs were included in the analysis. Variant counts (y-axis) have been log-transformed for ease of viewingBack to article page