chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	15411693	15411694	A	C	9	GENIC	homozygous	50073010
12	15412101	15412102	G	GA	6	GENIC	heterozygous	50073014
12	15412922	15412923	G	A	19	GENIC	homozygous	50568465
12	15415022	15415023	T	C	9	GENIC	homozygous	50436158
12	15417022	15417023	T	C	10	GENIC	homozygous	50073016
12	15417737	15417738	A	-	1	GENIC	homozygous	50560589
12	15417990	15417991	T	C	10	GENIC	homozygous	50436160
12	15418488	15418489	T	TA	3	GENIC	heterozygous	50436162
12	15419162	15419163	A	C	7	GENIC	heterozygous	50073036
12	15419306	15419307	G	A	11	GENIC	homozygous	50436164
12	15420081	15420082	G	A	12	GENIC	heterozygous	50073038
12	15420083	15420084	G	A	12	GENIC	heterozygous	50282106
12	15420085	15420086	A	G	11	GENIC	heterozygous	50282107
12	15420347	15420348	C	T	8	GENIC	homozygous	50073040
12	15420945	15420946	C	T	2	GENIC	heterozygous	50436166
12	15421064	15421065	T	A	2	GENIC	homozygous	50073056
12	15421706	15421707	C	T	6	GENIC	homozygous	50073058
12	15421946	15421947	A	C	18	GENIC	possibly homozygous	50073060
12	15422112	15422113	T	C	11	GENIC	homozygous	50073062
12	15422469	15422470	A	-	3	GENIC	heterozygous	50073066
12	15422960	15422961	T	C	15	GENIC	homozygous	50073068
12	15422985	15422986	A	G	19	GENIC	possibly homozygous	50073070
12	15424085	15424086	C	T	9	GENIC	homozygous	50073074
12	15424180	15424181	G	A	9	GENIC	possibly homozygous	50073076
12	15424694	15424695	C	T	1	GENIC	homozygous	50073080