chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	67546504	67546505	C	T	34	GENIC	homozygous	117711622
9	67547903	67547904	C	A	70	GENIC	homozygous	117711624
9	67549665	67549666	A	G	44	GENIC	homozygous	117711626
9	67551001	67551002	A	G	45	GENIC	homozygous	117551913
9	67551941	67551942	T	G	30	GENIC	possibly homozygous	117711630
9	67552273	67552274	T	C	43	GENIC	homozygous	117551919
9	67554437	67554438	T	C	18	GENIC	possibly homozygous	117824481
9	67554939	67554940	A	G	55	GENIC	homozygous	117551931
9	67556209	67556210	T	G	34	GENIC	homozygous	117551939
9	67556637	67556638	A	G	46	GENIC	possibly homozygous	117711632
9	67557330	67557331	G	A	23	GENIC	homozygous	117711634
9	67559507	67559508	G	C	47	GENIC	possibly homozygous	117551949
9	67561570	67561571	T	C	33	GENIC	homozygous	117711636
9	67562061	67562062	C	T	34	GENIC	possibly homozygous	117711638
9	67564080	67564081	G	C	45	GENIC	homozygous	117711640
9	67565146	67565147	T	G	46	GENIC	heterozygous	117711642
9	67565189	67565190	C	T	41	GENIC	heterozygous	117824482
9	67568015	67568016	A	G	53	GENIC	possibly homozygous	117711644
9	67568758	67568759	G	A	45	GENIC	homozygous	117711646
9	67570315	67570316	C	G	28	GENIC	homozygous	117711648
9	67570756	67570757	T	A	40	GENIC	homozygous	117711650
9	67570938	67570939	A	G	59	GENIC	homozygous	117711652
9	67573361	67573362	T	A	44	GENIC	possibly homozygous	117711654