chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90732709	90732710	C	T	41	GENIC	homozygous	116821053
10	90732754	90732755	A	G	32	GENIC	homozygous	116904879
10	90732832	90732833	C	A	27	GENIC	homozygous	116821055
10	90733690	90733691	A	T	37	GENIC	homozygous	116821057
10	90733875	90733876	G	A	26	GENIC	homozygous	116821059
10	90734102	90734103	C	A	38	GENIC	homozygous	116821063
10	90734824	90734825	T	C	42	GENIC	homozygous	116821065
10	90742019	90742020	T	C	28	GENIC	homozygous	116904887
10	90742979	90742980	T	C	30	GENIC	homozygous	116821077
10	90743040	90743041	T	G	28	GENIC	homozygous	116904891
10	90744994	90744995	T	G	19	GENIC	possibly homozygous	117180025
10	90746522	90746523	T	C	27	GENIC	homozygous	116821081
10	90748396	90748397	A	C	41	GENIC	homozygous	116821083
10	90745653	90745654	C	T	33	GENIC	homozygous	116951604
10	90741388	90741389	C	T	19	GENIC	homozygous	116951596
10	90741552	90741553	G	A	28	GENIC	homozygous	116951598
10	90742925	90742926	G	C	22	GENIC	homozygous	116951600
10	90745069	90745070	C	T	34	GENIC	homozygous	116951602