chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	175994702	175994703	A		37	GENIC	homozygous	135961645
2	175994815	175994816	C	T	60	GENIC	possibly homozygous	136374743
2	175995015	175995016	C	T	48	GENIC	homozygous	136374744
2	175995022	175995023	T	C	46	GENIC	homozygous	136374745
2	175995028	175995029	C	A	44	GENIC	homozygous	136374746
2	175995083	175995084	T	C	42	GENIC	homozygous	136374747
2	175995317	175995318	T	C	43	GENIC	homozygous	136374748
2	175995333	175995334	C	T	47	GENIC	homozygous	136374749
2	175995374	175995375	A	G	45	GENIC	homozygous	136374750
2	175995425	175995426	C	T	44	GENIC	homozygous	136374751
2	175995547	175995548	T	C	44	GENIC	homozygous	136374752
2	175995729	175995730	C	T	38	GENIC	possibly homozygous	136374753
2	175995731	175995732	C	T	38	GENIC	possibly homozygous	136374754
2	175995733	175995734	C	T	39	GENIC	homozygous	136374755
2	175995865	175995866	A	G	46	GENIC	homozygous	136374756
2	175996434	175996435	G	A	42	GENIC	homozygous	136374757
2	175996735	175996736	C	T	53	GENIC	homozygous	136374758
2	175997349	175997349		T	61	GENIC	homozygous	135961646
2	175998126	175998127	A	T	49	GENIC	homozygous	136374759
2	175998216	175998216		CCTTC	44	GENIC	homozygous	135961647
2	175998291	175998292	A	G	56	GENIC	homozygous	136374760
2	175998683	175998684	T	G	62	GENIC	homozygous	136374761