chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	16087538	16087539	C	T	34	GENIC	homozygous	117681162
9	16087543	16087544	C	T	33	GENIC	homozygous	117681164
9	16087557	16087558	A	G	35	GENIC	homozygous	117269006
9	16088536	16088537	G	T	23	GENIC	possibly homozygous	120452384
9	16088611	16088612	T	A	28	GENIC	homozygous	117681166
9	16088680	16088681	T	C	18	GENIC	homozygous	117269009
9	16089036	16089037	G	A	18	GENIC	homozygous	117681170
9	16089236	16089237	G	A	35	GENIC	homozygous	117269011
9	16089379	16089380	A	G	27	GENIC	possibly homozygous	117269012
9	16090761	16090762	A	C	20	GENIC	homozygous	117269016
9	16091046	16091047	G	A	20	GENIC	possibly homozygous	120452385
9	16091211	16091212	A	G	26	GENIC	homozygous	117269019
9	16091374	16091375	A	G	26	GENIC	possibly homozygous	117269021
9	16092073	16092074	A	G	23	GENIC	possibly homozygous	117269027
9	16092191	16092192	G	A	29	GENIC	possibly homozygous	120452386
9	16092221	16092222	C	T	27	GENIC	possibly homozygous	120452387
9	16092996	16092997	A	C	7	GENIC	homozygous	117269033
9	16093001	16093002	A	C	10	GENIC	homozygous	117461986
9	16093294	16093295	G	T	23	GENIC	homozygous	117269036
9	16093704	16093705	A	G	19	GENIC	homozygous	120452388
9	16093706	16093707	G	A	18	GENIC	homozygous	120452389
9	16291291	16291292	T	A	6	GENIC	homozygous	120385587
9	16291292	16291293	G	T	5	GENIC	homozygous	120385588
9	16359775	16359776	A	C	22	GENIC	homozygous	117269060
9	16385217	16385218	G	T	42	GENIC	homozygous	117269075
9	16385559	16385560	C	G	28	GENIC	homozygous	120452390
9	16385752	16385753	T	G	23	GENIC	homozygous	117681176
9	16385978	16385979	T	C	12	GENIC	homozygous	117269080