chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	96262563	96262564	T	C	45	GENIC	possibly homozygous	64662760
17	96265011	96265012	A	G	52	GENIC	homozygous	64662763
17	96265727	96265728	C	G	44	GENIC	homozygous	64662766
17	96269069	96269070	C	G	56	GENIC	homozygous	64662769
17	96272490	96272491	T	G	39	GENIC	homozygous	64662772
17	96274995	96274996	A	G	42	GENIC	homozygous	64662775
17	96280638	96280639	T	C	56	GENIC	possibly homozygous	64662778
17	96282044	96282045	C	G	52	GENIC	heterozygous	64662781
17	96282326	96282327	G	A	57	GENIC	heterozygous	64662784
17	96289230	96289231	A	G	59	GENIC	homozygous	64662787
17	96294168	96294169	A	G	73	GENIC	homozygous	64662789
17	96306396	96306397	G	A	52	GENIC	homozygous	64662792
17	96311202	96311203	G	A	58	GENIC	homozygous	64662795
17	96316250	96316251	C	T	42	GENIC	homozygous	64662798
17	96317270	96317271	G	A	34	GENIC	heterozygous	64662801
17	96319193	96319194	C	G	51	GENIC	homozygous	64662804
17	96282334	96282335	A	G	55	GENIC	heterozygous	64896555