chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	16087538	16087539	C	T	20	GENIC	homozygous	117681162
9	16087543	16087544	C	T	22	GENIC	homozygous	117681164
9	16087557	16087558	A	G	26	GENIC	homozygous	117269006
9	16088611	16088612	T	A	29	GENIC	homozygous	117681166
9	16088627	16088628	G	A	28	GENIC	homozygous	117681168
9	16088680	16088681	T	C	36	GENIC	homozygous	117269009
9	16089036	16089037	G	A	22	GENIC	homozygous	117681170
9	16089236	16089237	G	A	23	GENIC	homozygous	117269011
9	16091211	16091212	A	G	13	GENIC	homozygous	117269019
9	16091661	16091662	G	A	15	GENIC	possibly homozygous	117681172
9	16092996	16092997	A	C	13	GENIC	homozygous	117269033
9	16093001	16093002	A	C	11	GENIC	homozygous	117461986
9	16093045	16093046	A	C	10	GENIC	homozygous	117461987
9	16093046	16093047	C	T	10	GENIC	homozygous	117461988
9	16093294	16093295	G	T	19	GENIC	homozygous	117269036
9	16288395	16288396	A	T	19	GENIC	homozygous	120362501
9	16359775	16359776	A	C	33	GENIC	homozygous	117269060
9	16384842	16384843	G	A	19	GENIC	homozygous	117681174
9	16385217	16385218	G	T	15	GENIC	homozygous	117269075
9	16385535	16385536	T	C	32	GENIC	homozygous	117673863
9	16385646	16385647	T	C	27	GENIC	homozygous	117269078
9	16385752	16385753	T	G	38	GENIC	homozygous	117681176
9	16385978	16385979	T	C	10	GENIC	homozygous	117269080