chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	99813425	99813425		T	26	GENIC	homozygous	128736760
9	99813893	99813894	A	G	53	GENIC	homozygous	117617061
9	99813971	99813972	T	C	48	GENIC	homozygous	117617063
9	99814138	99814139	T	C	72	GENIC	homozygous	117617067
9	99814372	99814373	T	C	53	GENIC	possibly homozygous	117617069
9	99815481	99815482	T	C	45	GENIC	homozygous	117617075
9	99814085	99814086	C	G	66	GENIC	homozygous	120421772
9	99814161	99814162	C	A	65	GENIC	homozygous	120421773
9	99815378	99815379	C	T	55	GENIC	homozygous	120421774
9	99817777	99817778	T	C	62	GENIC	homozygous	117617083
9	99815770	99815771	G	T	52	GENIC	homozygous	117762936
9	99815892	99815893	G	A	51	GENIC	homozygous	120421775
9	99817529	99817530	A	G	51	GENIC	homozygous	117617079
9	99817669	99817670	C	T	66	GENIC	homozygous	117617081
9	99815820	99815824	ACAG		43	GENIC	homozygous	131454686
9	99817934	99817935	G	A	78	GENIC	homozygous	117617085
9	99817956	99817957	G	A	69	GENIC	homozygous	117617086