chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	74002849	74002850	T	C	16	GENIC	homozygous	116636043
10	74003090	74003091	T	C	25	GENIC	homozygous	116636045
10	74003499	74003500	A	T	18	GENIC	homozygous	116636047
10	74003736	74003737	T	C	29	GENIC	homozygous	116636049
10	74003737	74003738	G	A	29	GENIC	homozygous	116636051
10	74003761	74003762	C	T	24	GENIC	homozygous	116636053
10	74003761	74003761		T	24	GENIC	homozygous	128830695
10	74003776	74003777	G	A	24	GENIC	homozygous	116636055
10	74004436	74004437	A	G	32	GENIC	homozygous	116636057
10	74004788	74004792	TGGT		22	GENIC	homozygous	128830696
10	74005907	74005908	T	C	18	GENIC	homozygous	116636059
10	74006210	74006210		ACACAC	27	GENIC	homozygous	128830697
10	74008661	74008662	A	C	25	GENIC	homozygous	116636061
10	74009084	74009085	C	T	32	GENIC	homozygous	116636063
10	74010629	74010630	T	C	33	GENIC	homozygous	116636065
10	74011763	74011763		AA	21	GENIC	homozygous	128830698
10	74011942	74011943	G	A	23	GENIC	homozygous	116636067