chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59938173	59938176	AGA		54	GENIC	homozygous	146844217
8	59938551	59938552	G	C	49	GENIC	homozygous	146869740
8	59938557	59938558	A	T	49	GENIC	homozygous	146869741
8	59938599	59938600	A	G	43	GENIC	homozygous	146869742
8	59938608	59938609	C	A	46	GENIC	homozygous	146869743
8	59938623	59938624	T	C	46	GENIC	homozygous	146869744
8	59938626	59938628	TG		45	GENIC	homozygous	146844218
8	59938629	59938629		AT	46	GENIC	homozygous	146844219
8	59938647	59938648	G	C	44	GENIC	homozygous	146869745
8	59938673	59938674	G	T	44	GENIC	homozygous	146869746
8	59938705	59938706	G	A	42	GENIC	homozygous	141027868
8	59938854	59938855	C	G	41	GENIC	possibly homozygous	146869747
8	59938875	59938876	C	T	37	GENIC	homozygous	146869748
8	59938895	59938896	G	A	41	GENIC	homozygous	141027871
8	59938901	59938902	C	T	43	GENIC	homozygous	141027872
8	59938902	59938903	C	G	42	GENIC	homozygous	141027873
8	59939096	59939097	T	C	43	GENIC	homozygous	146869749
8	59941763	59941764	A	G	33	GENIC	homozygous	141027879
8	59943099	59943100	C	T	29	GENIC	homozygous	146869750
8	59938921	59938921		ACACTA	44	GENIC	homozygous	141015907
8	59938599	59938600	A		43	GENIC	heterozygous	404007608
8	59943173	59943174	G		33	GENIC	homozygous	141015909
8	59945751	59945752	C	T	35	GENIC	homozygous	141027884
8	59945783	59945784	G	A	34	GENIC	homozygous	146869752
8	59948759	59948760	T	C	37	GENIC	homozygous	141027887
8	59951284	59951285	G	C	42	GENIC	homozygous	141027890
8	59955540	59955541	G	A	44	GENIC	homozygous	141027893
8	59956706	59956707	C	T	48	GENIC	homozygous	146869753
8	59960918	59960919	G	T	35	GENIC	possibly homozygous	141027902