chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	49667106	49667107	T	C	69	GENIC	homozygous	140471088
19	49667837	49667838	T	C	72	GENIC	homozygous	140471089
19	49668437	49668438	A	G	81	GENIC	homozygous	140471090
19	49668593	49668594	G	T	28	GENIC	homozygous	403453372
19	49668593	49668594	G		28	GENIC	heterozygous	403453373
19	49668597	49668598	G	T	27	GENIC	homozygous	140471091
19	49668652	49668653	A	C	29	GENIC	homozygous	140471092
19	49668954	49668955	G	T	60	GENIC	homozygous	140471093
19	49668997	49668998	A	G	61	GENIC	homozygous	140471094
19	49669022	49669023	A	C	62	GENIC	homozygous	140471095
19	49669103	49669104	A	G	64	GENIC	homozygous	140471096
19	49669404	49669405	C	T	85	GENIC	homozygous	140471097
19	49671003	49671004	A	G	68	GENIC	possibly homozygous	140471098
19	49671287	49671288	C	T	71	GENIC	homozygous	140471099
19	49671727	49671728	G	T	31	GENIC	homozygous	140471100
19	49672031	49672032	C	A	67	GENIC	homozygous	140471101
19	49673333	49673333		TCAC	58	GENIC	homozygous	140393312
19	49669854	49669855	G		71	GENIC	homozygous	140393311