chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	149360460	149360461	G	C	22	GENIC	homozygous	111772080
3	149361659	149361660	G	A	14	GENIC	homozygous	111772082
3	149362438	149362439	G	A	27	GENIC	homozygous	111772084
3	149362814	149362815	T	A	25	GENIC	homozygous	111772086
3	149363479	149363480	C	T	30	GENIC	homozygous	111772088
3	149363908	149363909	A	C	26	GENIC	homozygous	111772090
3	149364628	149364629	G	A	26	GENIC	homozygous	111772092
3	149366075	149366076	G	T	25	GENIC	homozygous	111772094
3	149366106	149366107	C	T	18	GENIC	homozygous	111772096
3	149367075	149367076	T	C	20	GENIC	homozygous	111772098
3	149368566	149368567	C	T	26	GENIC	possibly homozygous	111772102
3	149368732	149368733	A	T	19	GENIC	homozygous	111772104
3	149369431	149369432	C	T	23	GENIC	homozygous	111772106
3	149371580	149371581	G	A	22	GENIC	homozygous	111772110
3	149372475	149372476	G	A	26	GENIC	homozygous	111772112
3	149373014	149373015	G	T	10	GENIC	homozygous	111772114
3	149373026	149373027	C	T	8	GENIC	homozygous	111772116
3	149373273	149373274	G	C	20	GENIC	homozygous	111772118
3	149373454	149373455	G	A	6	GENIC	homozygous	111772120
3	149373779	149373780	G	A	12	GENIC	homozygous	111772122
3	149375312	149375313	A	G	25	GENIC	possibly homozygous	111772124
3	149375321	149375322	T	C	24	GENIC	homozygous	111772126
3	149375457	149375458	C	T	26	GENIC	homozygous	111772128
3	149375587	149375588	A	G	28	GENIC	homozygous	111772130
3	149376454	149376455	T	C	15	GENIC	homozygous	111772132
3	149376591	149376592	G	A	17	GENIC	homozygous	111772134
3	149376677	149376678	A	T	12	GENIC	homozygous	111772136
3	149376876	149376877	C	T	17	GENIC	homozygous	111772138
3	149377007	149377008	A	G	15	GENIC	homozygous	111772140
3	149377061	149377062	T	C	17	GENIC	homozygous	111772142
3	149377076	149377077	C	T	17	GENIC	homozygous	111772144
3	149377197	149377198	G	A	11	GENIC	homozygous	111772146
3	149377732	149377733	G	A	18	GENIC	homozygous	111772148
3	149377838	149377839	C	T	16	GENIC	homozygous	111772150