28 lines (27 with data), 1.7 kB

##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##FILTER=<ID=RefCall,Description="Most likely reference">
##INFO=<ID=END,Number=1,Type=Integer,Description="Stop position of the interval">
##INFO=<ID=DB,Number=0,Type=Flag,Description="dbSNP membership",Source="dbSNP",Version="build 129">
##INFO=<ID=AC,Number=A,Type=Integer,Description="Allele counts">
##INFO=<ID=AF,Number=A,Type=Float,Description="Frequency of each ALT allele">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read depth of all passing filters reads.">
##FORMAT=<ID=MIN_DP,Number=1,Type=Integer,Description="Minimum DP observed within the GVCF block.">
##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Read depth of all passing filters reads for each allele.">
##FORMAT=<ID=VAF,Number=A,Type=Float,Description="Variant allele fractions.">
##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Genotype likelihoods, Phred encoded">
##FORMAT=<ID=PS,Number=1,Type=Integer,Description="Phase set">
##PEDIGREE=<Name_1="Val_1",Name_2="Val_2">
##pedigreeDb=http://my.pedigre.es
##contig=<ID=Chr1,length=50,description="Dog chromosome 1">
##contig=<ID=Chr2,length=25>
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	Fido	Spot
Chr1	21	DogSNP1	A	T	0	.	.	GT:GQ	0/1:.	0/1:42
Chr1	22	DogSNP2	A	T	0	.	.	GT:PL	0/1:.	0/1:10,0,20
Chr1	23	DogSNP3	A	T	0	.	.	GT:PL	0/1:.	0/1:10,0,20
Chr1	24	DogSNP4	A	T	0	.	.	GT:PL	0/1:10,0,20	0/1:10,0,20
Chr1	25	DogSNP5	A	T	0	.	.	GT:GQ:PL	0/1:42:10,0,20	0/1:42:10,0,20
Chr1	26	DogSNP6	A	T	.	.	.	GT:GQ:PL	0/1:42:990,90,0	0/1:42:9950,950,0
Chr1	27	DogSNP7	A	T	0	.	.	GT:PL	0/1:.	0/1:0,36,545