chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	83081321	83081322	A	G	51	GENIC	homozygous	116660480
10	83083602	83083603	A	T	21	GENIC	possibly homozygous	116813051
10	83083742	83083743	G	A	25	GENIC	homozygous	116813053
10	83084476	83084477	G	A	33	GENIC	homozygous	116813055
10	83084988	83084989	A	G	29	GENIC	homozygous	116813057
10	83085191	83085192	A	T	38	GENIC	homozygous	116813059
10	83085311	83085312	C	T	29	GENIC	possibly homozygous	116813061
10	83086260	83086261	T	C	4	GENIC	homozygous	117179853
10	83086264	83086265	T	C	3	GENIC	homozygous	117179854
10	83086481	83086482	C	T	33	GENIC	possibly homozygous	116813063
10	83086788	83086789	T	C	20	GENIC	homozygous	117086657
10	83087423	83087424	T	A	29	GENIC	homozygous	116813065
10	83087453	83087454	G	A	29	GENIC	homozygous	116813067
10	83087603	83087604	T	C	29	GENIC	homozygous	116813069
10	83087705	83087706	A	G	22	GENIC	possibly homozygous	116813071
10	83087834	83087835	A	C	23	GENIC	possibly homozygous	116813073
10	83087944	83087945	T	A	19	GENIC	possibly homozygous	116813075
10	83088068	83088069	T	C	26	GENIC	homozygous	116813077
10	83088493	83088494	G	A	30	GENIC	homozygous	116813079
10	83089016	83089017	C	T	30	GENIC	homozygous	116813081