chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41569015	41569016	T	G	22	GENIC	homozygous	115330640
12	41571365	41571366	G	A	17	GENIC	homozygous	115426986
12	41572509	41572510	T	C	20	GENIC	homozygous	115330683
12	41574365	41574366	C	G	21	GENIC	homozygous	115385488
12	41574733	41574734	T	C	33	GENIC	possibly homozygous	115704381
12	41574832	41574833	G	T	21	GENIC	homozygous	115330723
12	41579236	41579237	A	C	30	GENIC	homozygous	115330835
12	41579369	41579370	T	C	21	GENIC	heterozygous	118327203
12	41579373	41579374	T	C	20	GENIC	heterozygous	118327204
12	41579702	41579703	T	A	24	GENIC	homozygous	115330837
12	41581287	41581288	A	G	25	GENIC	homozygous	115426990
12	41582316	41582317	T	C	40	GENIC	homozygous	115330859
12	41586314	41586315	G	A	27	GENIC	homozygous	115330869
12	41586402	41586403	A	G	44	GENIC	homozygous	115385506
12	41586656	41586657	T	C	18	GENIC	homozygous	115330873
12	41586988	41586989	C	T	24	GENIC	homozygous	115385508
12	41587104	41587105	A	G	28	GENIC	homozygous	115385510
12	41587168	41587169	C	T	34	GENIC	homozygous	115385512
12	41587283	41587284	C	T	42	GENIC	homozygous	115385514
12	41587496	41587497	T	A	31	GENIC	homozygous	115330877
12	41582059	41582060	G	A	28	GENIC	homozygous	115442004