chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59595061	59595062	T	C	27	GENIC	homozygous	52664068
8	59596396	59596397	T	G	21	GENIC	homozygous	52983288
8	59596828	59596829	T	C	10	GENIC	homozygous	53388675
8	59596830	59596831	C	CAGTT	10	GENIC	homozygous	53388676
8	59596833	59596834	T	TAGAGCGC	11	GENIC	homozygous	53388677
8	59596835	59596836	T	TGC	11	GENIC	homozygous	53388678
8	59596999	59597058	TATTATAGGAAATAGATAATTTTACTTTTTCCTCTCCAGCTTGGATCAATTTTATTTAC	-----------------------------------------------------------	6	GENIC	homozygous	53388679
8	59597350	59597351	C	T	21	GENIC	homozygous	52983290
8	59597430	59597431	C	CAA	5	GENIC	homozygous	52664080
8	59598668	59598669	A	-	16	GENIC	homozygous	52983292
8	59603281	59603282	A	G	23	GENIC	homozygous	52664084
8	59603988	59603989	T	C	27	GENIC	homozygous	52664086
8	59604976	59604977	G	GAAAAAAAA	3	GENIC	heterozygous	53388680
8	59605092	59605093	T	-	7	GENIC	homozygous	52664090
8	59605240	59605241	T	-	16	GENIC	homozygous	53364020
8	59607059	59607060	C	T	31	GENIC	homozygous	52983293