##fileformat=VCFv4.3
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read depth">
##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Read depth for each allele">
##FORMAT=<ID=VAF,Number=A,Type=Float,Description="Variant allele fractions.">
##contig=<ID=chrM,length=16569>
##mitorsaw_version="0.2.7-8ee9b5b"
##mitorsaw_command="mitorsaw haplotype --reference human_GRCh38_no_alt_analysis_set.fasta --bam HG002.GRCh38.hifi_reads.bam --output-vcf HG002.GRCh38.mitorsaw.vcf.gz --output-hap-stats HG002.GRCh38.mitorsaw.json"
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	HG002
chrM	263	.	A	G	.	.	.	GT:DP:AD:VAF	1:611:0,610:1
chrM	302	.	A	AC	.	.	.	GT:DP:AD:VAF	1:610:50,556:0.91749173
chrM	310	.	T	TC	.	.	.	GT:DP:AD:VAF	1:609:42,566:0.9309211
chrM	456	.	C	T	.	.	.	GT:DP:AD:VAF	1:611:0,604:1
chrM	750	.	A	G	.	.	.	GT:DP:AD:VAF	1:621:0,615:1
chrM	1438	.	A	G	.	.	.	GT:DP:AD:VAF	1:629:0,629:1
chrM	3106	.	CN	C	.	.	.	GT:DP:AD:VAF	1:628:0,628:1
chrM	4336	.	T	C	.	.	.	GT:DP:AD:VAF	1:624:0,623:1
chrM	4769	.	A	G	.	.	.	GT:DP:AD:VAF	1:619:0,619:1
chrM	6800	.	A	G	.	.	.	GT:DP:AD:VAF	1:650:0,646:1
chrM	8557	.	G	A	.	.	.	GT:DP:AD:VAF	1:645:0,645:1
chrM	8860	.	A	G	.	.	.	GT:DP:AD:VAF	1:648:0,648:1
chrM	15175	.	C	T	.	.	.	GT:DP:AD:VAF	1:626:0,626:1
chrM	15326	.	A	G	.	.	.	GT:DP:AD:VAF	1:630:0,629:1
chrM	16304	.	T	C	.	.	.	GT:DP:AD:VAF	1:608:0,608:1
