chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	63676355	63676356	T	G	72	GENIC	homozygous	116616348
10	63678165	63678166	C	G	90	GENIC	homozygous	117062130
10	63680772	63680773	G	T	68	GENIC	homozygous	117062132
10	63682057	63682058	T	C	38	GENIC	homozygous	116616358
10	63682592	63682593	G	A	52	GENIC	homozygous	117062134
10	63684180	63684181	C	T	67	GENIC	homozygous	116940605
10	63685928	63685929	T	C	63	GENIC	homozygous	117062136
10	63688048	63688049	C	T	70	GENIC	homozygous	116616362
10	63688255	63688256	C	T	41	GENIC	homozygous	117062138
10	63690353	63690354	T	G	69	GENIC	homozygous	117062140
10	63692777	63692778	C	G	41	GENIC	possibly homozygous	117062142
10	63693832	63693833	G	T	50	GENIC	possibly homozygous	116616370
10	63694171	63694172	A	T	53	GENIC	homozygous	116940609
10	63694205	63694206	C		57	GENIC	homozygous	128824154
10	63694653	63694654	G	A	49	GENIC	homozygous	117062144
10	63697051	63697052	C	T	58	GENIC	homozygous	117062146
10	63701842	63701843	T	G	49	GENIC	homozygous	116616380
10	63703298	63703299	T	C	54	GENIC	homozygous	116616392
10	63703678	63703679	A	G	42	GENIC	homozygous	116616396
10	63703969	63703970	C	T	53	GENIC	homozygous	117062148
10	63704999	63705000	G	A	59	GENIC	homozygous	116791545
10	63708532	63708533	C	T	46	GENIC	homozygous	117062150
10	63709869	63709870	A	G	42	GENIC	homozygous	116616418
10	63711087	63711088	G	T	52	GENIC	homozygous	117062152
10	63712641	63712642	C	T	53	GENIC	homozygous	116791553
10	63712654	63712656	AG		55	GENIC	homozygous	133840838
10	63717992	63717995	AAG		35	GENIC	homozygous	128824162