Targeted summary stats.

pos_id: unique GRCh38 variant ID. chromosome - 9-digit position - ref allele - alt allele, chrom: chromosome, pos: GRCh38 position, ref: reference allele, alt: alternate allele, qual: PHRED quality score, filter: filter status, faf95_gnomad: 95%CI filtering allele frequency from gnomAD, faf95_gnomad_ancestry: ancestry group contributing the filtering allele frequency, incon_faf95: 95%CI filtering allele frequency from internal controls, vpspr_ac: allele count in VPSPr cases, vpspr_an: allele number in VPSPr cases, af_pseudo: allele frequency for plotting purposes (AF = 0 is plotted as AF = 1e-6 to enable log scale plotting).
(TSV)