chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	60928831	60928832	A	C	18	GENIC	homozygous	60212349
2	60929886	60929887	T	C	16	GENIC	possibly homozygous	59810849
2	60930439	60930440	G	T	23	GENIC	homozygous	60212350
2	60930547	60930548	A	G	27	GENIC	possibly homozygous	59810850
2	60931163	60931164	T	G	13	GENIC	heterozygous	60212351
2	60931211	60931212	A	T	20	GENIC	possibly homozygous	59810854
2	60931414	60931415	T	G	21	GENIC	homozygous	60212352
2	60931743	60931744	T	A	9	GENIC	possibly homozygous	59810855
2	60931898	60931899	T	C	20	GENIC	possibly homozygous	59810856
2	60931693	60931694	A	G	8	GENIC	homozygous	60113536
2	60931721	60931722	A	T	13	GENIC	homozygous	60113537
2	60932965	60932966	T	C	13	GENIC	homozygous	60212353
2	60933111	60933112	A	C	9	GENIC	homozygous	59810863
2	60933259	60933260	C	T	25	GENIC	homozygous	59810864