chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	172200174	172200175	G	C	19	GENIC	homozygous	119746075
3	172200612	172200613	C	G	19	GENIC	homozygous	112208943
3	172201826	172201827	C	T	15	GENIC	homozygous	119746076
3	172201848	172201849	A	C	16	GENIC	homozygous	112208945
3	172201977	172201978	A	G	19	GENIC	homozygous	119746077
3	172202006	172202007	A	G	18	GENIC	homozygous	112208949
3	172202007	172202008	T	C	18	GENIC	homozygous	112208951
3	172202749	172202750	C	A	22	GENIC	homozygous	119746078
3	172202980	172202981	T	C	20	GENIC	homozygous	112208953
3	172204535	172204536	C	T	21	GENIC	homozygous	119746079
3	172204807	172204808	G	A	13	GENIC	homozygous	120000432
3	172204811	172204812	G	A	12	GENIC	homozygous	119746081
3	172204815	172204816	A	G	12	GENIC	homozygous	112208957
3	172204911	172204912	G	A	19	GENIC	homozygous	119746082
3	172206486	172206487	C	A	12	GENIC	homozygous	119746083
3	172206514	172206515	A	G	14	GENIC	homozygous	112208961
3	172206690	172206691	T	C	16	GENIC	homozygous	112208963
3	172207118	172207119	T	C	18	GENIC	homozygous	112208965
3	172207469	172207470	G	A	16	GENIC	homozygous	119746084
3	172207643	172207644	C	A	15	GENIC	homozygous	119746085