chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59346921	59346922	A	G	42	GENIC	homozygous	116607992
10	59349377	59349378	T	C	12	GENIC	homozygous	116607996
10	59350054	59350055	A	G	42	GENIC	homozygous	116607998
10	59352041	59352042	G	T	13	GENIC	homozygous	116608000
10	59352045	59352046	C	A	15	GENIC	homozygous	116608002
10	59352836	59352837	C	T	36	GENIC	homozygous	117079548
10	59353174	59353175	C	T	27	GENIC	homozygous	117079550
10	59353547	59353548	C	T	29	GENIC	homozygous	116608004
10	59354861	59354862	A	G	32	GENIC	homozygous	117079551
10	59355037	59355038	A	G	21	GENIC	homozygous	116608006
10	59355960	59355961	A	G	44	GENIC	homozygous	116608008
10	59356794	59356795	G	A	26	GENIC	homozygous	116788448
10	59357012	59357013	C	T	27	GENIC	homozygous	116608010
10	59357013	59357014	A	G	28	GENIC	homozygous	116608012
10	59357477	59357478	C	T	19	GENIC	homozygous	117079553
10	59358113	59358114	C	T	23	GENIC	homozygous	117079555
10	59359288	59359289	T	C	29	GENIC	possibly homozygous	117079556