chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	70300076	70300077	A	G	28	GENIC	homozygous	111264412
17	70301133	70301134	A	G	30	GENIC	homozygous	111264414
17	70301800	70301801	C	T	10	GENIC	homozygous	111359164
17	70301982	70301983	T	C	19	GENIC	homozygous	111359166
17	70302324	70302325	G	C	21	GENIC	homozygous	111359168
17	70303432	70303433	A	G	34	GENIC	homozygous	111359170
17	70304966	70304967	G	C	21	GENIC	homozygous	111359172
17	70305028	70305029	G	T	35	GENIC	homozygous	111264416
17	70305778	70305779	G	A	32	GENIC	homozygous	111359174
17	70306605	70306606	A	G	7	GENIC	homozygous	111656387
17	70310013	70310014	T	C	36	GENIC	homozygous	111264422
17	70311487	70311488	A	C	14	GENIC	homozygous	111359176
17	70315498	70315499	A	G	3	GENIC	homozygous	111656389
17	70316082	70316083	T	C	39	GENIC	homozygous	111264428
17	70316665	70316666	G	A	20	GENIC	homozygous	111359180
17	70317793	70317794	G	A	27	GENIC	possibly homozygous	111264432
17	70319815	70319816	T	C	8	GENIC	possibly homozygous	111656391
17	70322006	70322007	A	C	29	GENIC	homozygous	111359182
17	70323510	70323511	C	T	31	GENIC	homozygous	111359184
17	70324767	70324768	T	C	24	GENIC	homozygous	111264442