chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	17041469	17041470	A	G	33	GENIC	homozygous	117681914
9	17043260	17043261	A	T	39	GENIC	homozygous	117681916
9	17044490	17044491	C	T	38	GENIC	homozygous	117681918
9	17045573	17045574	G	A	29	GENIC	homozygous	117681920
9	17046732	17046733	A	G	39	GENIC	homozygous	117270069
9	17048053	17048054	G	A	37	GENIC	possibly homozygous	117681922
9	17048646	17048647	T	A	48	GENIC	homozygous	117270071
9	17048694	17048695	T	A	51	GENIC	homozygous	117270072
9	17049138	17049139	G	C	37	GENIC	homozygous	117681924
9	17049328	17049329	G	A	26	GENIC	possibly homozygous	117681926
9	17050735	17050736	T	C	27	GENIC	homozygous	117270073
9	17051741	17051742	T	C	15	GENIC	homozygous	117674816
9	17052025	17052026	G	A	21	GENIC	possibly homozygous	117270075
9	17052353	17052354	T	C	23	GENIC	homozygous	117270077
9	17053012	17053013	G	A	24	GENIC	homozygous	117681928
9	17053059	17053060	G	A	21	GENIC	homozygous	117674820
9	17053205	17053206	G	A	26	GENIC	homozygous	117681930
9	17053417	17053418	A	G	30	GENIC	homozygous	117674824
9	17053727	17053728	T	G	28	GENIC	homozygous	117681932
9	17053947	17053948	C	T	42	GENIC	homozygous	117681934
9	17054398	17054399	A	G	42	GENIC	possibly homozygous	117681936
9	17054523	17054524	A	T	29	GENIC	possibly homozygous	117681938
9	17054654	17054655	G	C	36	GENIC	possibly homozygous	117681940
9	17054855	17054856	A	G	21	GENIC	homozygous	117681942
9	17055299	17055300	T	C	45	GENIC	homozygous	117681944
9	17055476	17055477	G	C	32	GENIC	possibly homozygous	117674840
9	17055638	17055639	T	C	42	GENIC	homozygous	117681946
9	17055735	17055736	A	G	56	GENIC	possibly homozygous	117681948
9	17055944	17055945	A	G	39	GENIC	homozygous	117681950
9	17056724	17056725	T	G	20	GENIC	homozygous	117681952
9	17058693	17058694	T	C	33	GENIC	possibly homozygous	117681954
9	17058986	17058987	A	G	32	GENIC	homozygous	117270083
9	17060387	17060388	G	A	33	GENIC	possibly homozygous	117681956