##fileformat=VCFv4.0
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth (only filtered reads used for calling)">
##FORMAT=<ID=GQ,Number=1,Type=Float,Description="Genotype Quality">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=PL,Number=3,Type=Float,Description="Normalized, Phred-scaled likelihoods for AA,AB,BB genotypes where A=ref and B=alt; not applicable if site is not biallelic">
##INFO=<ID=AC,Number=.,Type=Integer,Description="Allele count in genotypes, for each ALT allele, in the same order as listed">
##INFO=<ID=AF,Number=.,Type=Float,Description="Allele Frequency, for each ALT allele, in the same order as listed">
##INFO=<ID=AN,Number=1,Type=Integer,Description="Total number of alleles in called genotypes">
##INFO=<ID=DBSNP129,Number=0,Type=Flag,Description="DBSNP129 Membership">
##INFO=<ID=DBSNP132,Number=0,Type=Flag,Description="DBSNP132 Membership">
##INFO=<ID=GenericAnnotation,Number=1,Type=Integer,Description="For each variant in the 'variants' ROD, finds all entries in the other -B files that overlap the variant's position.">
##INFO=<ID=HAPMAP,Number=0,Type=Flag,Description="HAPMAP Membership">
##INFO=<ID=OMNI,Number=0,Type=Flag,Description="OMNI Membership">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	HG00513	NA12045	HG00625