chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	18385349	18385350	T	C	12	GENIC	possibly homozygous	50091792
12	18386028	18386031	GCC	---	1	GENIC	homozygous	50507249
12	18386171	18386173	TT	--	2	GENIC	heterozygous	50507251
12	18386174	18386181	CTCCTCT	-------	3	GENIC	heterozygous	50507253
12	18386327	18386328	A	G	17	GENIC	homozygous	50091812
12	18386484	18386485	T	C	16	GENIC	homozygous	50091814
12	18386699	18386700	C	T	19	GENIC	homozygous	50091816
12	18386960	18386961	T	C	14	GENIC	homozygous	50091818
12	18387104	18387105	T	C	26	GENIC	possibly homozygous	50091820
12	18387132	18387133	A	G	26	GENIC	homozygous	50091822
12	18387260	18387261	A	-	2	GENIC	heterozygous	50091824
12	18388772	18388773	A	T	2	GENIC	heterozygous	50091840
12	18388951	18388952	A	G	15	GENIC	homozygous	50091842
12	18389023	18389024	T	C	20	GENIC	homozygous	50091844
12	18390162	18390163	T	G	21	GENIC	homozygous	50091852
12	18390232	18390233	T	C	3	GENIC	heterozygous	50091858
12	18390398	18390402	TCTA	----	2	GENIC	homozygous	50091860
12	18390579	18390580	T	-	2	GENIC	heterozygous	50091862
12	18390728	18390729	A	G	8	GENIC	possibly homozygous	50091864
12	18390875	18390876	G	A	18	GENIC	heterozygous	50091866
12	18390908	18390909	A	G	16	GENIC	homozygous	50091868
12	18391023	18391024	C	-	15	GENIC	homozygous	50091870