chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	60929070	60929071	A	T	20	GENIC	homozygous	59810844
2	60929086	60929087	T	C	20	GENIC	homozygous	59810845
2	60929211	60929212	T	TTA	20	GENIC	homozygous	59810846
2	60929265	60929266	T	G	23	GENIC	homozygous	59810848
2	60929886	60929887	T	C	30	GENIC	homozygous	59810849
2	60930547	60930548	A	G	38	GENIC	homozygous	59810850
2	60930719	60930720	G	A	26	GENIC	homozygous	59810851
2	60930858	60930859	A	G	18	GENIC	homozygous	59810852
2	60931211	60931212	A	T	29	GENIC	homozygous	59810854
2	60931743	60931744	T	A	24	GENIC	homozygous	59810855
2	60931898	60931899	T	C	18	GENIC	homozygous	59810856
2	60932121	60932122	T	A	30	GENIC	homozygous	59810857
2	60932183	60932184	A	G	21	GENIC	homozygous	59810858
2	60932689	60932690	C	T	25	GENIC	homozygous	59810859
2	60932703	60932704	A	G	25	GENIC	homozygous	59810860
2	60933003	60933004	A	AACACACACAC	10	GENIC	homozygous	60481726
2	60933032	60933033	G	A	13	GENIC	homozygous	59810861
2	60933039	60933040	A	AACACAC	12	GENIC	homozygous	60481727
2	60933111	60933112	A	C	20	GENIC	homozygous	59810863
2	60933259	60933260	C	T	19	GENIC	homozygous	59810864