chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59595061	59595062	T	C	19	GENIC	homozygous	52664068
8	59596828	59596829	T	C	23	GENIC	homozygous	53388675
8	59596830	59596831	C	CAGTT	22	GENIC	homozygous	53388676
8	59596833	59596834	T	TAGAGCGC	22	GENIC	homozygous	53388677
8	59596835	59596836	T	TGC	21	GENIC	homozygous	53388678
8	59596874	59596875	G	GA	6	GENIC	heterozygous	53433223
8	59596999	59597058	TATTATAGGAAATAGATAATTTTACTTTTTCCTCTCCAGCTTGGATCAATTTTATTTAC	-----------------------------------------------------------	4	GENIC	homozygous	53388679
8	59597430	59597431	C	CA	27	GENIC	possibly homozygous	52664082
8	59597430	59597431	C	CAAA	27	GENIC	heterozygous	52983291
8	59603281	59603282	A	G	28	GENIC	homozygous	52664084
8	59603988	59603989	T	C	34	GENIC	homozygous	52664086
8	59604976	59604977	G	GAAAAAAAA	24	GENIC	heterozygous	53388680
8	59604977	59604978	A	-	24	GENIC	heterozygous	52664088
8	59605092	59605093	T	-	15	GENIC	homozygous	52664090
8	59605239	59605241	TT	--	22	GENIC	heterozygous	53550752
8	59605240	59605241	T	-	22	GENIC	possibly homozygous	53364020
8	59605922	59605923	G	A	15	GENIC	possibly homozygous	52664094
8	59606599	59606600	A	AAAAC	39	GENIC	homozygous	52664096