chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	21066943	21066944	A	G	11	GENIC	homozygous	111338201
17	21066961	21066962	G	A	20	GENIC	homozygous	111177881
17	21067291	21067292	G	A	20	GENIC	homozygous	111177883
17	21067963	21067964	G	A	29	GENIC	homozygous	111177885
17	21068639	21068640	G	A	33	GENIC	homozygous	111177887
17	21068724	21068725	T	A	21	GENIC	homozygous	110986821
17	21069391	21069392	A	G	18	GENIC	homozygous	110986823
17	21071248	21071249	T	C	28	GENIC	homozygous	110986859
17	21072479	21072480	T	C	33	GENIC	homozygous	111177889
17	21072851	21072852	C	T	23	GENIC	homozygous	110986884
17	21073123	21073124	T	C	38	GENIC	possibly homozygous	110986887
17	21073162	21073163	G	A	26	GENIC	homozygous	111177891
17	21073409	21073410	G	A	23	GENIC	homozygous	110986889
17	21073712	21073713	G	T	24	GENIC	homozygous	110986891
17	21073726	21073727	A	T	27	GENIC	possibly homozygous	110986893
17	21073763	21073764	A	G	27	GENIC	homozygous	110986895
17	21073776	21073777	C	T	28	GENIC	homozygous	110986897
17	21073794	21073795	C	T	25	GENIC	homozygous	110986899