chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	174150686	174150687	A	T	35	GENIC	homozygous	145379491
2	174150990	174150991	A	T	40	GENIC	homozygous	145379492
2	174151480	174151481	T	C	40	GENIC	homozygous	142964914
2	174152749	174152750	C	T	51	GENIC	homozygous	145379493
2	174154395	174154396	C	T	28	GENIC	homozygous	136372764
2	174156824	174156825	C	T	34	GENIC	homozygous	136372765
2	174159113	174159114	G	T	26	GENIC	homozygous	142964927
2	174161025	174161026	C	A	45	GENIC	homozygous	136372766
2	174161182	174161183	C	A	25	GENIC	homozygous	136372767
2	174162896	174162897	T	G	45	GENIC	homozygous	136372770
2	174163252	174163253	A	C	41	GENIC	homozygous	136372771
2	174164742	174164743	T	A	29	GENIC	possibly homozygous	136372775
2	174165431	174165432	A	T	51	GENIC	homozygous	142964938
2	174165720	174165721	C	T	42	GENIC	homozygous	145379494
2	174166034	174166035	G	A	45	GENIC	homozygous	136372776
2	174169044	174169045	G	A	59	GENIC	homozygous	145379495
2	174175145	174175146	A	G	40	GENIC	homozygous	142964946
2	174175739	174175740	A	G	37	GENIC	possibly homozygous	145379496
2	174176903	174176904	G	A	45	GENIC	homozygous	136372779
2	174170831	174170832	A		29	GENIC	homozygous	135961088
2	174175922	174175922		A	42	GENIC	homozygous	135961089
2	174162783	174162783		TGTA	39	GENIC	homozygous	145348627
2	174166588	174166588		T	27	GENIC	possibly homozygous	145348628
2	174172638	174172641	CAA		25	GENIC	homozygous	145348629