chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	58860653	58860654	G	A	30	GENIC	possibly homozygous	116788012
10	58861718	58861719	G	A	59	GENIC	homozygous	117011697
10	58862047	58862048	G	A	57	GENIC	homozygous	116788014
10	58862792	58862793	A	G	18	GENIC	heterozygous	118039612
10	58862807	58862808	G	A	13	GENIC	heterozygous	118039613
10	58862823	58862824	C	A	11	GENIC	possibly homozygous	118039614
10	58862877	58862878	G	A	25	GENIC	heterozygous	118039615
10	58862886	58862887	C	T	19	GENIC	possibly homozygous	118039616
10	58863359	58863360	T	C	63	GENIC	homozygous	116788016
10	58864659	58864660	T	C	74	GENIC	homozygous	116788018
10	58864705	58864706	G	A	70	GENIC	homozygous	116788020
10	58865074	58865075	A	C	61	GENIC	homozygous	116788022
10	58865180	58865181	C	G	62	GENIC	homozygous	116788024
10	58865868	58865869	G	C	52	GENIC	possibly homozygous	116788026
10	58866407	58866408	T	C	66	GENIC	possibly homozygous	116788028
10	58866590	58866591	A	C	69	GENIC	homozygous	116788030
10	58867098	58867099	A	G	60	GENIC	homozygous	116788032
10	58867691	58867692	C	T	46	GENIC	heterozygous	118039617
10	58867712	58867713	A	G	31	GENIC	possibly homozygous	117011698
10	58869295	58869296	T	C	59	GENIC	possibly homozygous	116788034
10	58870218	58870219	T	C	42	GENIC	homozygous	117011699
10	58870843	58870844	G	A	59	GENIC	homozygous	116788036
10	58871397	58871398	A	C	45	GENIC	homozygous	116788038
10	58872202	58872203	A	G	47	GENIC	homozygous	116607414
10	58872337	58872338	T	C	70	GENIC	homozygous	116788040
10	58872487	58872488	C	T	65	GENIC	possibly homozygous	117011700
10	58872766	58872767	C	A	22	GENIC	homozygous	118039618