chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	15411693	15411694	A	C	20	GENIC	possibly homozygous	50073010
12	15412101	15412102	G	GA	5	GENIC	heterozygous	50073014
12	15413405	15413406	C	T	27	GENIC	possibly homozygous	50436156
12	15415022	15415023	T	C	23	GENIC	possibly homozygous	50436158
12	15417022	15417023	T	C	20	GENIC	homozygous	50073016
12	15417990	15417991	T	C	24	GENIC	homozygous	50436160
12	15419162	15419163	A	C	17	GENIC	possibly homozygous	50073036
12	15419306	15419307	G	A	26	GENIC	homozygous	50436164
12	15420081	15420082	G	A	11	GENIC	homozygous	50073038
12	15420083	15420084	G	A	11	GENIC	homozygous	50282106
12	15420085	15420086	A	G	12	GENIC	homozygous	50282107
12	15420347	15420348	C	T	24	GENIC	possibly homozygous	50073040
12	15420812	15420813	G	A	3	GENIC	homozygous	50073042
12	15420827	15420828	G	A	4	GENIC	heterozygous	50073044
12	15420945	15420946	C	T	7	GENIC	heterozygous	50436166
12	15421032	15421033	T	A	1	GENIC	homozygous	50073046
12	15421035	15421036	T	G	1	GENIC	homozygous	50073048
12	15421056	15421057	A	C	2	GENIC	homozygous	50073054
12	15421064	15421065	T	A	4	GENIC	homozygous	50073056
12	15421145	15421146	G	GCTCGTCTGGACGCTCTCTATCTTGTCT	2	GENIC	homozygous	50504041
12	15421052	15421053	G	C	1	GENIC	homozygous	50504040
12	15421706	15421707	C	T	19	GENIC	heterozygous	50073058
12	15421946	15421947	A	C	21	GENIC	homozygous	50073060
12	15422112	15422113	T	C	20	GENIC	homozygous	50073062
12	15422469	15422470	A	-	7	GENIC	possibly homozygous	50073066
12	15422960	15422961	T	C	24	GENIC	homozygous	50073068
12	15422985	15422986	A	G	19	GENIC	homozygous	50073070
12	15424085	15424086	C	T	14	GENIC	homozygous	50073074
12	15424180	15424181	G	A	22	GENIC	possibly homozygous	50073076
12	15424680	15424681	T	G	1	GENIC	homozygous	50073078
12	15424694	15424695	C	T	2	GENIC	homozygous	50073080