chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	32647983	32647984	A	C	13	GENIC	possibly homozygous	50312939
12	32647989	32647990	C	G	14	GENIC	homozygous	50175785
12	32647990	32647991	A	G	13	GENIC	homozygous	50175786
12	32648851	32648852	T	C	55	GENIC	possibly homozygous	50175787
12	32649028	32649030	TG	--	3	GENIC	homozygous	50175788
12	32649167	32649168	A	G	64	GENIC	homozygous	50175789
12	32649490	32649491	A	AAGG	25	GENIC	homozygous	50175790
12	32649582	32649583	A	G	22	GENIC	heterozygous	50175791
12	32649597	32649598	A	G	24	GENIC	heterozygous	50175792
12	32649600	32649601	A	G	23	GENIC	heterozygous	50175793
12	32657087	32657088	G	GC	34	GENIC	homozygous	50175795
12	32657096	32657098	GA	--	31	GENIC	homozygous	50175796
12	32657112	32657113	T	G	33	GENIC	homozygous	50175797
12	32657115	32657116	A	G	29	GENIC	possibly homozygous	50175798