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##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth (reads with MQ=255 or with bad mates are filtered)">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Normalized, Phred-scaled likelihoods for genotypes as defined in the VCF specification">
##INFO=<ID=AC,Number=A,Type=Integer,Description="Allele count in genotypes, for each ALT allele, in the same order as listed">
##contig=<ID=chr8,length=145138636>
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT D2406015 D2415554 D2415559
chr8 130407414 . G A 73.29 . AC=3 GT:AD:DP:GQ:PL 1/1:0,2:2:6:49,6,0 0/1:2,2:4:37:37,0,37 ./.:0,0:.:.:.
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