##fileformat=VCFv4.2
##fileDate=20150729
##source=custom
##reference=genome.fa
##phasing=none
##INFO=<ID=AN,Number=1,Type=Integer,Description="Total number of alleles in called genotypes">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total read depth at the locus">
##INFO=<ID=MQ,Number=1,Type=Float,Description="RMS Mapping Quality">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=AD,Number=2,Type=Integer,Description="# of reads supporting consensus reference/indel at the site">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Total coverage at the site">
##FORMAT=<ID=MMQ,Number=A,Type=Integer,Description="median mapping quality">
##FILTER=<ID=LowQual,Description="Low quality">
##FILTER=<ID=PASS,Description="All filters passed">
##FILTER=<ID=REJECT,Description="Not somatic due to normal call frequency or phred likelihoods: tumor: 35, normal 35.">
##contig=<ID=chr1,length=249250621>
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	Blank
