chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	82033719	82033720	G	C	44	GENIC	homozygous	117587129
9	82034970	82034971	A	C	54	GENIC	homozygous	117587131
9	82035957	82035958	G	T	57	GENIC	homozygous	117587133
9	82036570	82036571	T	A	51	GENIC	homozygous	117587135
9	82036651	82036652	T	C	53	GENIC	possibly homozygous	117587137
9	82036655	82036656	G	T	56	GENIC	possibly homozygous	117587139
9	82037766	82037767	G	A	69	GENIC	homozygous	117587141
9	82038086	82038087	T	C	49	GENIC	homozygous	117587143
9	82038334	82038335	G	T	63	GENIC	homozygous	117587145
9	82038994	82038995	C	T	54	GENIC	homozygous	117587147
9	82039497	82039498	A	G	68	GENIC	homozygous	117587149
9	82040608	82040609	C	A	35	GENIC	heterozygous	117587151
9	82041166	82041167	T	G	61	GENIC	homozygous	117587153
9	82041321	82041322	C	T	48	GENIC	homozygous	117587155
9	82041574	82041575	T	C	67	GENIC	heterozygous	117587157
9	82041743	82041744	A	G	47	GENIC	possibly homozygous	117587159
9	82042036	82042037	A	G	64	GENIC	homozygous	117587161
9	82042669	82042670	C	T	49	GENIC	homozygous	117587163
9	82043353	82043354	A	T	46	GENIC	homozygous	117587165
9	82043521	82043522	T	G	77	GENIC	possibly homozygous	117587167
9	82044706	82044707	T	G	67	GENIC	homozygous	117587169
9	82045838	82045839	C	A	35	GENIC	heterozygous	117587171