chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	18385349	18385350	T	C	22	GENIC	homozygous	50091792
12	18386327	18386328	A	G	9	GENIC	homozygous	50091812
12	18386484	18386485	T	C	14	GENIC	homozygous	50091814
12	18386699	18386700	C	T	22	GENIC	homozygous	50091816
12	18386960	18386961	T	C	16	GENIC	homozygous	50091818
12	18387104	18387105	T	C	16	GENIC	homozygous	50091820
12	18387132	18387133	A	G	20	GENIC	homozygous	50091822
12	18388484	18388485	C	T	10	GENIC	homozygous	50091828
12	18388486	18388487	C	T	10	GENIC	homozygous	50091830
12	18388497	18388498	A	AT	11	GENIC	homozygous	50091832
12	18388498	18388499	A	AT	11	GENIC	homozygous	50091834
12	18388772	18388773	A	T	8	GENIC	homozygous	50091840
12	18388951	18388952	A	G	16	GENIC	homozygous	50091842
12	18389023	18389024	T	C	11	GENIC	homozygous	50091844
12	18389223	18389224	C	CT	10	GENIC	homozygous	50091846
12	18390162	18390163	T	G	9	GENIC	homozygous	50091852
12	18390232	18390233	T	C	8	GENIC	homozygous	50091858
12	18390728	18390729	A	G	21	GENIC	homozygous	50091864
12	18390875	18390876	G	A	17	GENIC	homozygous	50091866
12	18390908	18390909	A	G	16	GENIC	homozygous	50091868
12	18391023	18391024	C	-	8	GENIC	homozygous	50091870
12	18390578	18390579	T	-	7	GENIC	homozygous	51060431