chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	54328214	54328215	A	G	28	GENIC	homozygous	117994600
10	54328301	54328302	C	G	51	GENIC	homozygous	117994601
10	54328640	54328641	G	A	40	GENIC	homozygous	116600094
10	54328829	54328830	T	C	33	GENIC	homozygous	116600096
10	54328916	54328917	G	C	55	GENIC	homozygous	116600098
10	54330732	54330733	G	A	72	GENIC	homozygous	116600100
10	54331174	54331175	G	A	48	GENIC	homozygous	116600102
10	54331937	54331938	C	T	52	GENIC	homozygous	116600104
10	54332065	54332066	G	C	54	GENIC	homozygous	116600106
10	54332344	54332345	A	G	55	GENIC	homozygous	116600108
10	54334614	54334615	T	C	27	GENIC	homozygous	116600110
10	54334686	54334687	C	T	26	GENIC	heterozygous	117994602
10	54334921	54334922	A	T	48	GENIC	homozygous	116600112
10	54334994	54334995	A	G	60	GENIC	homozygous	116600114
10	54335100	54335101	C	T	52	GENIC	possibly homozygous	116600116
10	54335338	54335339	A	G	31	GENIC	homozygous	116600118
10	54335620	54335621	G	C	14	GENIC	possibly homozygous	117994603
10	54336028	54336029	G	C	44	GENIC	homozygous	116600120
10	54336956	54336957	T	G	53	GENIC	possibly homozygous	116600122
10	54337752	54337753	G	T	35	GENIC	homozygous	116600124
10	54337870	54337871	G	T	28	GENIC	homozygous	116600126
10	54338299	54338300	A	G	47	GENIC	homozygous	116600128
10	54338575	54338576	C	A	43	GENIC	homozygous	116600130
10	54339373	54339374	C	T	39	GENIC	homozygous	116600132
10	54340300	54340301	G	T	69	GENIC	homozygous	116600134
10	54341062	54341063	A	G	34	GENIC	possibly homozygous	116600136
10	54341123	54341124	G	A	34	GENIC	homozygous	116600140
10	54341944	54341945	C	T	57	GENIC	homozygous	116600142
10	54342675	54342676	C	T	51	GENIC	homozygous	116600144
10	54342875	54342876	C	G	33	GENIC	heterozygous	117994604
10	54342877	54342878	C	G	31	GENIC	heterozygous	117994605