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/usr/lib/R/site-library/VariantAnnotation/unitTests/cases/FORMAT_header_no_SAMPLEs.vcf is in r-bioc-variantannotation 1.20.2-1+b1.

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##fileformat=VCFv4.1
##INFO=<ID=AN,Number=1,Type=Integer,Description="Total Allele Count">
##ALT=<ID=DEL,Description="Deletion">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=DS,Number=1,Type=Float,Description="Genotype dosage from MaCH/Thunder">
##FORMAT=<ID=GL,Number=.,Type=Float,Description="Genotype Likelihoods">
##reference=GRCh37
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO
1	10523	.	TCCG	T	62	PASS	AN=2184
1	10583	rs58108140	G	A	100	PASS	AN=2184
1	10611	rs189107123	C	G	100	PASS	AN=2184
1	10616	.	CCGCCGTTGCAAAGGCGCGCCG	C	172	PASS	AN=2184
1	11540	.	T	TA	30	PASS	AN=2184