##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##reference=file://grch37.chr20.fa.gz
##contig=<ID=1,length=249250621>
##contig=<ID=16,length=249250621>
##contig=<ID=17,length=249250621>
##contig=<ID=20,length=249250621>
##contig=<ID=21,length=249250621>
##ALT=<ID=*,Description="Represents allele(s) other than observed.">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Raw read depth">
##INFO=<ID=MQ0F,Number=1,Type=Float,Description="Fraction of MQ0 reads (smaller is better)">
##INFO=<ID=I16,Number=16,Type=Float,Description="Auxiliary tag used for calling, see description of bcf_callret1_t in bam2bcf.h">
##INFO=<ID=QS,Number=R,Type=Float,Description="Auxiliary tag used for calling">
##FORMAT=<ID=PL,Number=G,Type=Integer,Description="List of Phred-scaled genotype likelihoods">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	sample
1	1368833	.	T	<*>	0	.	DP=1;I16=0,1,0,0,13,169,0,0,60,3600,0,0,3,9,0,0;QS=1,0;MQ0F=0	PL	0,3,13
1	1368833	.	TAAAAAAAAAAAAAAAA	TAAAAAAAAAAAAAA	0	.	DP=2;I16=0,1,1,0,10,100,30,900,60,3600,60,3600,3,9,25,625;QS=0.5,0.5	PL	6,0,6
1	1370000	.	C	T,G,A	0	.	DP=11;I16=11,0,0,0,452,18594,0,0,319,9251,0,0,223,4959,0,0;QS=1,1,0,1,1;MQ0F=0	PL	0,0,0,0,0,0,.,.,.,.
