chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	150819762	150819763	C	T	17	GENIC	homozygous	108301625
1	150826623	150826624	A	T	78	GENIC	heterozygous	108749166
1	150826647	150826648	C	T	75	GENIC	heterozygous	108749167
1	150858355	150858356	C	T	71	GENIC	possibly homozygous	108301633
1	150890630	150890631	A	C	67	GENIC	homozygous	108301635
1	150891164	150891165	T	G	38	GENIC	homozygous	108301637
1	150904732	150904733	A	G	6	GENIC	homozygous	108749168
1	150922657	150922658	C	A	92	GENIC	heterozygous	108749169
1	150922687	150922688	T	G	98	GENIC	heterozygous	108749170
1	150923958	150923959	C	A	10	GENIC	homozygous	108749171
1	150937423	150937424	C	T	43	GENIC	homozygous	108301639
1	150937469	150937470	T	C	49	GENIC	homozygous	108301641
1	150937492	150937493	C	T	49	GENIC	homozygous	108301643
1	150938367	150938368	A	G	58	GENIC	homozygous	108301645
1	150939788	150939789	A	C	71	GENIC	possibly homozygous	108301649
1	150940736	150940737	T	A	72	GENIC	homozygous	108301651
1	150942130	150942131	T	C	47	GENIC	possibly homozygous	108301653
1	150942174	150942175	T	G	42	GENIC	homozygous	108301655
1	150942436	150942437	G	C	61	GENIC	possibly homozygous	108301657
1	150953942	150953943	G	A	76	GENIC	possibly homozygous	108301665
1	150949306	150949307	C	G	60	GENIC	possibly homozygous	108301659
1	150952415	150952416	T	C	57	GENIC	homozygous	108301661
1	150952859	150952860	T	C	60	GENIC	possibly homozygous	108301663
1	150960638	150960639	T	C	68	GENIC	possibly homozygous	108301667
1	150961030	150961031	G	C	78	GENIC	homozygous	108301669
1	150970938	150970939	G	A	82	GENIC	heterozygous	108749172
1	150970946	150970947	G	A	91	GENIC	heterozygous	108749173
1	150970954	150970955	G	A	89	GENIC	heterozygous	108749174
1	150970958	150970959	G	A	88	GENIC	heterozygous	108749175
1	150970962	150970963	G	A	86	GENIC	heterozygous	108301671
1	150973309	150973310	G	A	59	GENIC	homozygous	108301673
1	150975040	150975041	T	A	59	GENIC	homozygous	108301675