File: contrast.1.1.out

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bcftools 1.16-1
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##fileformat=VCFv4.0
##FILTER=<ID=PASS,Description="All filters passed">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##contig=<ID=2,length=62435964>
##INFO=<ID=NOVELAL,Number=.,Type=String,Description="List of samples with novel alleles. Note that samples listed here are not listed in NOVELGT again.">
##INFO=<ID=NOVELGT,Number=.,Type=String,Description="List of samples with novel genotypes">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	A	B
2	280	.	T	A	246	.	.	GT	0/0	0/0
2	280	.	T	A	246	.	NOVELAL=B	GT	0/0	0/1
2	280	.	T	A	246	.	NOVELAL=B	GT	0/0	1/1