chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41569804	41569805	C	T	21	GENIC	homozygous	115426982
12	41570202	41570203	T	C	18	GENIC	homozygous	115426984
12	41571365	41571366	G	A	24	GENIC	homozygous	115426986
12	41572509	41572510	T	C	14	GENIC	homozygous	115330683
12	41574365	41574366	C	G	20	GENIC	homozygous	115385488
12	41578200	41578201	C	T	22	GENIC	homozygous	115426988
12	41579236	41579237	A	C	22	GENIC	homozygous	115330835
12	41579702	41579703	T	A	14	GENIC	homozygous	115330837
12	41581287	41581288	A	G	14	GENIC	homozygous	115426990
12	41582316	41582317	T	C	34	GENIC	homozygous	115330859
12	41586314	41586315	G	A	34	GENIC	homozygous	115330869
12	41586656	41586657	T	C	30	GENIC	homozygous	115330873
12	41586988	41586989	C	T	22	GENIC	possibly homozygous	115385508
12	41587104	41587105	A	G	27	GENIC	homozygous	115385510
12	41587168	41587169	C	T	38	GENIC	homozygous	115385512
12	41587283	41587284	C	T	25	GENIC	homozygous	115385514
12	41587496	41587497	T	A	25	GENIC	homozygous	115330877