chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	141725985	141725986	T	C	35	GENIC	homozygous	54838938
7	141726584	141726585	C	T	29	GENIC	homozygous	54838940
7	141727681	141727682	C	T	34	GENIC	homozygous	54838942
7	141727864	141727865	T	C	37	GENIC	homozygous	54838944
7	141727902	141727906	GTGT	----	17	GENIC	heterozygous	55017230
7	141727904	141727906	GT	--	17	GENIC	heterozygous	55017232
7	141727946	141727947	G	C	28	GENIC	homozygous	54159581
7	141727992	141727993	A	ATGTGCGTGTGTGTGTGCGCATGTGTGTC	42	GENIC	homozygous	55017234
7	141728018	141728019	C	CTG	27	GENIC	possibly homozygous	54838946
7	141728898	141728899	G	GGACATGCTGTCATCATAGTGGGGAGCACGGCAGCACACAGGCGGACATGCTGTCGTGTAGTGGGGAGCACGGCAGCACACAGGCA	32	GENIC	homozygous	55017236
7	141728998	141728999	A	-	56	GENIC	homozygous	54159585
7	141731958	141731959	T	C	27	GENIC	homozygous	54159590