chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	100453096	100453097	C	T	47	GENIC	homozygous	120421873
9	100456362	100456363	G	A	43	GENIC	homozygous	120421874
9	100458959	100458960	G	A	30	GENIC	homozygous	117619642
9	100462101	100462102	C	A	43	GENIC	homozygous	117763741
9	100462434	100462435	C	T	40	GENIC	homozygous	120421875
9	100462506	100462507	T	A	31	GENIC	homozygous	117619644
9	100463061	100463062	A	G	63	GENIC	homozygous	117619646
9	100463918	100463919	C	T	56	GENIC	homozygous	117619648
9	100465789	100465790	A	T	56	GENIC	homozygous	117619652
9	100466497	100466498	A	G	65	GENIC	homozygous	117619656
9	100466730	100466731	T	C	50	GENIC	homozygous	117619658
9	100469095	100469096	G	T	37	GENIC	homozygous	117619664
9	100469550	100469551	C	T	55	GENIC	homozygous	120421876
9	100470261	100470262	T	C	38	GENIC	homozygous	117619668
9	100470796	100470797	C	T	68	GENIC	homozygous	120421877
9	100470916	100470917	G	A	41	GENIC	homozygous	117619670
9	100471780	100471781	C	T	28	GENIC	homozygous	117619674
9	100475569	100475570	G	A	29	GENIC	homozygous	120421878
9	100476874	100476875	T	A	28	GENIC	homozygous	117619680
9	100477784	100477785	T	C	39	GENIC	homozygous	117619682
9	100478119	100478120	T	C	74	GENIC	homozygous	117619684
9	100478906	100478907	T	C	60	GENIC	homozygous	117619686
9	100479484	100479485	A	G	37	GENIC	homozygous	117619688