chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	61658886	61658887	T	C	25	GENIC	homozygous	125353884
18	61659867	61659868	A	C	25	GENIC	homozygous	125353886
18	61661833	61661834	C	T	15	GENIC	homozygous	125353887
18	61662194	61662195	A	T	32	GENIC	homozygous	125353889
18	61662695	61662696	A	G	31	GENIC	homozygous	125353891
18	61664491	61664492	T	C	24	GENIC	homozygous	125353893
18	61665306	61665307	A	T	19	GENIC	homozygous	125353895
18	61665613	61665614	C	G	10	GENIC	homozygous	125353896
18	61665786	61665787	A	G	16	GENIC	homozygous	125353898
18	61666026	61666027	T	A	27	GENIC	homozygous	125353900
18	61666152	61666153	A	G	20	GENIC	homozygous	125353901
18	61666375	61666376	A	G	20	GENIC	homozygous	125353903
18	61667541	61667542	A	G	21	GENIC	homozygous	125353907
18	61668152	61668153	G	A	16	GENIC	homozygous	125353908
18	61668800	61668801	A	G	20	GENIC	homozygous	125353910
18	61670535	61670536	A	C	4	GENIC	homozygous	125353912
18	61670801	61670802	T	G	32	GENIC	homozygous	125353916
18	61670826	61670827	C	T	29	GENIC	homozygous	125353918
18	61672369	61672370	A	G	11	GENIC	homozygous	125391076
18	61672635	61672636	T	C	26	GENIC	homozygous	125353920
18	61671993	61671994	C	A	6	GENIC	heterozygous	125403866