chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	21066943	21066944	A	G	19	GENIC	homozygous	111338201
17	21066961	21066962	G	A	21	GENIC	homozygous	111177881
17	21067291	21067292	G	A	21	GENIC	homozygous	111177883
17	21067963	21067964	G	A	31	GENIC	homozygous	111177885
17	21068639	21068640	G	A	26	GENIC	homozygous	111177887
17	21068724	21068725	T	A	22	GENIC	homozygous	110986821
17	21069391	21069392	A	G	28	GENIC	homozygous	110986823
17	21071248	21071249	T	C	20	GENIC	homozygous	110986859
17	21072479	21072480	T	C	21	GENIC	homozygous	111177889
17	21072851	21072852	C	T	19	GENIC	homozygous	110986884
17	21073123	21073124	T	C	22	GENIC	homozygous	110986887
17	21073162	21073163	G	A	21	GENIC	homozygous	111177891
17	21073409	21073410	G	A	20	GENIC	homozygous	110986889
17	21073712	21073713	G	T	39	GENIC	homozygous	110986891
17	21073726	21073727	A	T	39	GENIC	homozygous	110986893
17	21073763	21073764	A	G	45	GENIC	homozygous	110986895
17	21073776	21073777	C	T	43	GENIC	homozygous	110986897
17	21073794	21073795	C	T	39	GENIC	possibly homozygous	110986899