chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	96260551	96260552	A	C	3	GENIC	homozygous	65453898
17	96262563	96262564	T	C	10	GENIC	homozygous	64662760
17	96262760	96262760		A	17	GENIC	homozygous	65453900
17	96263782	96263783	G	T	5	GENIC	homozygous	65453902
17	96265011	96265012	A	G	22	GENIC	homozygous	64662763
17	96265727	96265728	C	G	23	GENIC	homozygous	64662766
17	96269069	96269070	C	G	16	GENIC	homozygous	64662769
17	96263301	96263302	T		16	GENIC	heterozygous	65365488
17	96274995	96274996	A	G	30	GENIC	homozygous	64662775
17	96280638	96280639	T	C	12	GENIC	homozygous	64662778
17	96282048	96282049	C	G	6	GENIC	homozygous	65453904
17	96289230	96289231	A	G	25	GENIC	homozygous	64662787
17	96294168	96294169	A	G	25	GENIC	homozygous	64662789
17	96297186	96297187	A		22	GENIC	heterozygous	65164799
17	96303266	96303269	TGT		27	GENIC	heterozygous	65164801
17	96306396	96306397	G	A	18	GENIC	homozygous	64662792
17	96311202	96311203	G	A	11	GENIC	homozygous	64662795
17	96316250	96316251	C	T	20	GENIC	homozygous	64662798
17	96319193	96319194	C	G	16	GENIC	homozygous	64662804