chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	219362681	219362682	T	C	26	GENIC	homozygous	108993895
1	219363175	219363176	G	A	43	GENIC	homozygous	108993896
1	219363698	219363699	G	A	31	GENIC	homozygous	108993897
1	219364768	219364769	G	T	43	GENIC	homozygous	108993898
1	219365601	219365602	T	C	25	GENIC	homozygous	108993899
1	219366837	219366838	C	T	27	GENIC	homozygous	108993900
1	219367916	219367917	C	T	17	GENIC	homozygous	108993902
1	219367943	219367944	T	C	25	GENIC	possibly homozygous	108993903
1	219368944	219368945	A	C	35	GENIC	possibly homozygous	108993904
1	219370871	219370872	A	G	14	GENIC	homozygous	108540625
1	219371516	219371517	T	C	32	GENIC	homozygous	108540629
1	219372326	219372327	G	A	10	GENIC	homozygous	108993905
1	219373001	219373002	A	G	42	GENIC	homozygous	108540631
1	219373680	219373681	G	C	26	GENIC	homozygous	108993906