chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	69990864	69990865	C	T	31	GENIC	homozygous	109290747
1	69994723	69994724	G	A	35	GENIC	homozygous	109102416
1	69995343	69995344	C	T	35	GENIC	homozygous	109290748
1	69996637	69996638	T	A	28	GENIC	homozygous	109102423
1	69996975	69996976	T	C	19	GENIC	homozygous	109102425
1	69999284	69999285	T	C	38	GENIC	homozygous	109102433
1	69999855	69999856	A	G	34	GENIC	homozygous	109102435
1	69999905	69999906	C	A	30	GENIC	homozygous	109290749
1	70001618	70001619	G	A	26	GENIC	homozygous	109290750
1	70001729	70001730	G	C	42	GENIC	homozygous	109290751
1	70002165	70002166	G	T	21	GENIC	homozygous	109290752
1	70002199	70002200	G	A	26	GENIC	homozygous	109290753
1	70002928	70002929	T	G	25	GENIC	homozygous	109102439
1	70002960	70002961	T	A	22	GENIC	homozygous	109102441
1	70003091	70003092	C	G	30	GENIC	homozygous	109290755
1	70003980	70003981	C	T	28	GENIC	homozygous	109102443
1	70004031	70004032	T	C	25	GENIC	homozygous	109290756
1	70004667	70004668	T	C	19	GENIC	homozygous	109102445
1	70004717	70004718	C	T	18	GENIC	homozygous	109290758
1	70004723	70004724	G	A	21	GENIC	homozygous	109290759
1	70014941	70014942	A	C	33	GENIC	homozygous	109102481
1	70017220	70017221	T	C	29	GENIC	homozygous	109102483