chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	217040705	217040706	G	A	19	GENIC	homozygous	109193698
1	217048051	217048052	T	A	5	GENIC	heterozygous	109193700
1	217048347	217048348	A	G	22	GENIC	homozygous	109193702
1	217048900	217048901	T	C	30	GENIC	homozygous	108992538
1	217049404	217049405	G	A	14	GENIC	homozygous	108992543
1	217049496	217049497	T	A	15	GENIC	homozygous	108992544
1	217050037	217050038	G	T	21	GENIC	homozygous	108992545
1	217050783	217050784	G	T	29	GENIC	homozygous	109193704
1	217051154	217051155	A	G	32	GENIC	possibly homozygous	108992547
1	217052345	217052346	A	G	26	GENIC	possibly homozygous	108992550
1	217053571	217053572	A	G	27	GENIC	homozygous	108992551
1	217054347	217054348	G	T	15	GENIC	possibly homozygous	109193708
1	217055064	217055065	C	T	25	GENIC	homozygous	109193710
1	217055400	217055401	T	C	26	GENIC	homozygous	109193712
1	217055583	217055584	A	T	30	GENIC	homozygous	108992554
1	217056931	217056932	C	T	26	GENIC	homozygous	108992555
1	217060120	217060121	A	T	19	GENIC	homozygous	108992558
1	217061955	217061956	A	G	21	GENIC	homozygous	109193714
1	217062350	217062351	C	A	25	GENIC	homozygous	108992560
1	217063110	217063111	A	C	26	GENIC	homozygous	108992561
1	217065247	217065248	G	A	30	GENIC	homozygous	109193717
1	217066288	217066289	T	C	16	GENIC	homozygous	108992564