##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##reference=file://hs38DH.fa
##contig=<ID=chr20,length=64444167>
##ALT=<ID=*,Description="Represents allele(s) other than observed.">
##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">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Number of high-quality bases">
##INFO=<ID=END,Number=1,Type=Integer,Description="End position of the variant described in this record">
##INFO=<ID=MinDP,Number=1,Type=Integer,Description="Minimum per-sample depth in this gVCF block">
##contig=<ID=chr1,length=248956422>
##contig=<ID=chr2,length=242193529>
##contig=<ID=chr3,length=198295559>
##contig=<ID=chr4,length=190214555>
##contig=<ID=chr5,length=181538259>
##contig=<ID=chr6,length=170805979>
##contig=<ID=chr7,length=159345973>
##contig=<ID=chr8,length=145138636>
##contig=<ID=chr9,length=138394717>
##contig=<ID=chr10,length=133797422>
##contig=<ID=chr11,length=135086622>
##contig=<ID=chr12,length=133275309>
##contig=<ID=chr13,length=114364328>
##contig=<ID=chr14,length=107043718>
##contig=<ID=chr15,length=101991189>
##contig=<ID=chr16,length=90338345>
##contig=<ID=chr17,length=83257441>
##contig=<ID=chr18,length=80373285>
##contig=<ID=chr19,length=58617616>
##contig=<ID=chr21,length=46709983>
##contig=<ID=chr22,length=50818468>
##contig=<ID=chrX,length=156040895>
##contig=<ID=chrY,length=57227415>
##contig=<ID=chrM,length=16569>
##INFO=<ID=INDEL,Number=0,Type=Flag,Description="Indicates that the variant is an INDEL.">
##INFO=<ID=IDV,Number=1,Type=Integer,Description="Maximum number of reads supporting an indel">
##INFO=<ID=IMF,Number=1,Type=Float,Description="Maximum fraction of reads supporting an indel">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Raw read depth">
##INFO=<ID=VDB,Number=1,Type=Float,Description="Variant Distance Bias for filtering splice-site artefacts in RNA-seq data (bigger is better)",Version="3">
##INFO=<ID=RPB,Number=1,Type=Float,Description="Mann-Whitney U test of Read Position Bias (bigger is better)">
##INFO=<ID=MQB,Number=1,Type=Float,Description="Mann-Whitney U test of Mapping Quality Bias (bigger is better)">
##INFO=<ID=BQB,Number=1,Type=Float,Description="Mann-Whitney U test of Base Quality Bias (bigger is better)">
##INFO=<ID=MQSB,Number=1,Type=Float,Description="Mann-Whitney U test of Mapping Quality vs Strand Bias (bigger is better)">
##INFO=<ID=SGB,Number=1,Type=Float,Description="Segregation based metric.">
##INFO=<ID=MQ0F,Number=1,Type=Float,Description="Fraction of MQ0 reads (smaller is better)">
##FORMAT=<ID=SP,Number=1,Type=Integer,Description="Phred-scaled strand bias P-value">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	SampleA	SampleB
chr20	6281864	.	C	<*>	.	.	END=6281908;MinDP=1;QS=1,0	PL:DP	0,3,27:1	.:.
chr20	6281909	.	T	<*>	0	.	MQ0F=0;DP=2;I16=0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0;MinDP=1;QS=1,0	PL:DP:SP	0,3,27:1:.	0,0,0:0:0
chr20	6281910	.	A	<*>	.	.	END=6281930;MinDP=1;QS=1,0	PL:DP	.:.	0,3,25:1
chr20	6283321	.	T	<*>	.	.	END=6283435;MinDP=4;QS=1,0	PL:DP	.:.	0,12,14:4
chr20	6283436	.	G	A,<*>	0	.	VDB=0.154358;SGB=-0.511536;RPB=1;MQB=1;MQSB=1;BQB=1;MQ0F=0;DP=4;I16=0,1,2,1,37,1369,87,2619,3,9,9,27,9,81,71,1691;QS=0.25,0.75,0	PL:DP:SP	.:.:.	6,5,0,9,9,7:4:0
chr20	6283437	.	A	<*>	.	.	END=6283744;MinDP=2;QS=1,0	PL:DP	.:.	0,6,22:2
chr20	6283999	.	C	<*>	.	.	END=6284344;MinDP=1;QS=1,0	PL:DP	0,3,4:1	.:.
