chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59595061	59595062	T	C	28	GENIC	homozygous	52664068
8	59596396	59596397	T	G	35	GENIC	homozygous	52983288
8	59596828	59596829	T	A	4	GENIC	homozygous	52664070
8	59596829	59596830	T	G	4	GENIC	homozygous	52664072
8	59596834	59596835	T	TG	3	GENIC	homozygous	52664074
8	59596884	59596885	C	A	16	GENIC	homozygous	52664076
8	59596887	59596889	AA	--	6	GENIC	heterozygous	52983289
8	59597057	59597058	C	A	18	GENIC	heterozygous	52664078
8	59597350	59597351	C	T	43	GENIC	homozygous	52983290
8	59597430	59597431	C	CAA	28	GENIC	possibly homozygous	52664080
8	59597430	59597431	C	CA	28	GENIC	heterozygous	52664082
8	59597430	59597431	C	CAAA	28	GENIC	heterozygous	52983291
8	59598668	59598669	A	-	48	GENIC	homozygous	52983292
8	59603281	59603282	A	G	30	GENIC	possibly homozygous	52664084
8	59603988	59603989	T	C	32	GENIC	homozygous	52664086
8	59605239	59605240	T	-	35	GENIC	homozygous	52664092
8	59607059	59607060	C	T	46	GENIC	homozygous	52983293