chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90732709	90732710	C	T	33	GENIC	homozygous	116821053
10	90732754	90732755	A	G	45	GENIC	homozygous	116904879
10	90732832	90732833	C	A	28	GENIC	homozygous	116821055
10	90733690	90733691	A	T	43	GENIC	homozygous	116821057
10	90733875	90733876	G	A	24	GENIC	homozygous	116821059
10	90733892	90733893	C	A	23	GENIC	homozygous	116821061
10	90734102	90734103	C	A	35	GENIC	homozygous	116821063
10	90734824	90734825	T	C	26	GENIC	homozygous	116821065
10	90735140	90735141	C	A	25	GENIC	homozygous	116821067
10	90735396	90735397	G	A	29	GENIC	homozygous	116821069
10	90735762	90735763	C	T	27	GENIC	homozygous	116821071
10	90739918	90739919	C	T	43	GENIC	homozygous	117087901
10	90740030	90740031	T	C	32	GENIC	homozygous	116821073
10	90742019	90742020	T	C	28	GENIC	homozygous	116904887
10	90742979	90742980	T	C	31	GENIC	homozygous	116821077
10	90743040	90743041	T	G	40	GENIC	homozygous	116904891
10	90743884	90743885	A	G	9	GENIC	homozygous	116821079
10	90744074	90744075	C	T	32	GENIC	homozygous	117087903
10	90747738	90747739	A	T	17	GENIC	homozygous	117087905