chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	172195462	172195463	C	T	22	GENIC	homozygous	112258444
3	172197657	172197658	T	C	28	GENIC	homozygous	112208938
3	172200431	172200432	A	T	29	GENIC	homozygous	112208939
3	172200450	172200451	G	A	29	GENIC	homozygous	112208941
3	172200612	172200613	C	G	34	GENIC	homozygous	112208943
3	172201848	172201849	A	C	33	GENIC	homozygous	112208945
3	172201938	172201939	C	G	38	GENIC	homozygous	112208947
3	172202006	172202007	A	G	46	GENIC	homozygous	112208949
3	172202007	172202008	T	C	47	GENIC	homozygous	112208951
3	172202980	172202981	T	C	21	GENIC	homozygous	112208953
3	172204791	172204792	A	C	55	GENIC	heterozygous	112208955
3	172204815	172204816	A	G	53	GENIC	heterozygous	112208957
3	172204821	172204822	G	A	55	GENIC	heterozygous	112258445
3	172205947	172205948	A	G	38	GENIC	homozygous	112208959
3	172206514	172206515	A	G	32	GENIC	homozygous	112208961
3	172206690	172206691	T	C	42	GENIC	possibly homozygous	112208963
3	172207118	172207119	T	C	30	GENIC	homozygous	112208965
3	172204762	172204763	T	C	50	GENIC	heterozygous	112449829