chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59595061	59595062	T	C	30	GENIC	homozygous	52664068
8	59596828	59596829	T	C	10	GENIC	homozygous	53388675
8	59596830	59596831	C	CAGTT	8	GENIC	homozygous	53388676
8	59596833	59596834	T	TAGAGCGC	8	GENIC	homozygous	53388677
8	59596835	59596836	T	TGC	8	GENIC	homozygous	53388678
8	59596874	59596875	G	GA	1	GENIC	homozygous	53433223
8	59596999	59597058	TATTATAGGAAATAGATAATTTTACTTTTTCCTCTCCAGCTTGGATCAATTTTATTTAC	-----------------------------------------------------------	4	GENIC	homozygous	53388679
8	59597430	59597431	C	CA	13	GENIC	possibly homozygous	52664082
8	59603281	59603282	A	G	19	GENIC	homozygous	52664084
8	59603988	59603989	T	C	23	GENIC	homozygous	52664086
8	59604977	59604978	A	-	17	GENIC	heterozygous	52664088
8	59605092	59605093	T	-	16	GENIC	heterozygous	52664090
8	59605240	59605241	T	-	12	GENIC	possibly homozygous	53364020
8	59605922	59605923	G	A	13	GENIC	homozygous	52664094
8	59606599	59606600	A	AAAAC	14	GENIC	homozygous	52664096