chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59937097	59937098	G	C	57	GENIC	homozygous	142076193
8	59938702	59938703	T	C	29	GENIC	homozygous	141027867
8	59938729	59938730	T	C	39	GENIC	homozygous	141027869
8	59938389	59938390	G	A	61	GENIC	possibly homozygous	141027865
8	59938699	59938700	C	A	27	GENIC	homozygous	141027866
8	59938705	59938706	G	A	29	GENIC	homozygous	141027868
8	59938733	59938734	T	C	43	GENIC	homozygous	141027870
8	59938895	59938896	G	A	46	GENIC	homozygous	141027871
8	59938901	59938902	C	T	44	GENIC	homozygous	141027872
8	59938902	59938903	C	G	45	GENIC	homozygous	141027873
8	59939720	59939721	T	A	62	GENIC	homozygous	141027876
8	59940104	59940105	A	G	43	GENIC	homozygous	141027877
8	59941090	59941091	C	T	59	GENIC	homozygous	141027878
8	59941763	59941764	A	G	53	GENIC	homozygous	141027879
8	59943089	59943090	C	T	56	GENIC	homozygous	142076194
8	59938735	59938735		T	43	GENIC	homozygous	141015906
8	59938921	59938921		ACACTA	45	GENIC	homozygous	141015907
8	59943920	59943921	G	A	51	GENIC	homozygous	142076195
8	59945751	59945752	C	T	64	GENIC	homozygous	141027884
8	59946717	59946718	A	T	52	GENIC	possibly homozygous	141027885
8	59955540	59955541	G	A	58	GENIC	homozygous	141027893
8	59948759	59948760	T	C	46	GENIC	homozygous	141027887
8	59949763	59949764	G	A	40	GENIC	homozygous	142076196
8	59951284	59951285	G	C	54	GENIC	homozygous	141027890
8	59956045	59956046	C	A	56	GENIC	homozygous	142076197
8	59956494	59956495	A	G	48	GENIC	homozygous	141027896
8	59956753	59956754	T	G	59	GENIC	possibly homozygous	141027897
8	59958466	59958467	G	A	53	GENIC	homozygous	142076198
8	59959021	59959022	T	C	47	GENIC	homozygous	141027899
8	59960918	59960919	G	T	64	GENIC	possibly homozygous	141027902