chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13348599	13348600	A	G	58	GENIC	homozygous	116495794
10	13348793	13348794	G	T	57	GENIC	homozygous	116495796
10	13348983	13348984	T	C	48	GENIC	homozygous	116495798
10	13349739	13349740	T	G	46	GENIC	homozygous	116994648
10	13349862	13349863	G	A	34	GENIC	homozygous	117982276
10	13349905	13349906	C	T	38	GENIC	homozygous	117982278
10	13349953	13349954	T	G	42	GENIC	homozygous	117982280
10	13349974	13349975	C	A	30	GENIC	homozygous	116994649
10	13349978	13349979	T	C	30	GENIC	homozygous	117982281
10	13349983	13349984	A	G	30	GENIC	homozygous	116994650
10	13349984	13349985	T	C	32	GENIC	homozygous	117407982
10	13350030	13350031	G	A	48	GENIC	homozygous	116735729
10	13350132	13350133	T	C	48	GENIC	homozygous	116495800
10	13350139	13350140	G	A	47	GENIC	possibly homozygous	116495802
10	13350642	13350643	A	G	32	GENIC	homozygous	116495804
10	13350813	13350814	G	A	43	GENIC	homozygous	116495806
10	13350870	13350871	T	C	51	GENIC	homozygous	116495808
10	13350877	13350878	T	C	49	GENIC	homozygous	116495810
10	13351111	13351112	G	A	61	GENIC	homozygous	116495816
10	13351176	13351177	C	T	26	GENIC	homozygous	116495818
10	13351213	13351214	G	A	45	GENIC	homozygous	116495820
10	13351379	13351380	A	G	46	GENIC	homozygous	116495822
10	13351569	13351570	T	G	47	GENIC	homozygous	116495824
10	13351898	13351899	G	A	51	GENIC	homozygous	116495826
10	13352343	13352344	T	C	43	GENIC	homozygous	116495828
10	13354357	13354358	A	C	68	GENIC	homozygous	116495830
10	13354694	13354695	T	C	53	GENIC	heterozygous	116495832