chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	44627067	44627068	G	A	53	GENIC	homozygous	111054035
17	44628308	44628309	G	A	41	GENIC	homozygous	111054037
17	44629942	44629943	A	G	49	GENIC	homozygous	111054039
17	44632269	44632270	T	C	69	GENIC	homozygous	111054041
17	44632328	44632329	A	T	52	GENIC	homozygous	111054043
17	44637026	44637027	G	A	38	GENIC	homozygous	111204053
17	44637404	44637405	G	T	10	GENIC	homozygous	119289814
17	44637097	44637098	G	A	9	GENIC	homozygous	119289810
17	44637123	44637124	G	A	21	GENIC	homozygous	119289811
17	44637672	44637673	G	A	10	GENIC	homozygous	119289815
17	44637790	44637791	T	G	41	GENIC	possibly homozygous	119289816
17	44637813	44637814	C	A	42	GENIC	homozygous	119289817
17	44640861	44640862	T	G	46	GENIC	homozygous	111054045
17	44641002	44641003	A	G	28	GENIC	homozygous	119289818
17	44641709	44641710	T	G	15	GENIC	possibly homozygous	111054047
17	44641711	44641712	T	G	16	GENIC	homozygous	111054049
17	44642875	44642876	G	C	62	GENIC	homozygous	111054051
17	44645442	44645443	A	C	36	GENIC	homozygous	111054053
17	44645497	44645498	G	T	65	GENIC	homozygous	111054055