chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	87342539	87342540	A	G	17	GENIC	homozygous	116949580
10	87342648	87342649	C	T	18	GENIC	homozygous	116949582
10	87342663	87342664	G	A	19	GENIC	homozygous	116949584
10	87342995	87342996	T	C	7	GENIC	homozygous	116899340
10	87343081	87343082	A	G	27	GENIC	homozygous	116899344
10	87343693	87343694	C	T	25	GENIC	homozygous	116949588
10	87344248	87344249	T	C	24	GENIC	possibly homozygous	116949590
10	87346167	87346168	A	G	25	GENIC	homozygous	116669656
10	87343131	87343132	T	C	40	GENIC	homozygous	116982379
10	87347648	87347649	C	T	23	GENIC	homozygous	116949592
10	87347828	87347829	T	G	17	GENIC	homozygous	116669658
10	87348050	87348051	A	C	35	GENIC	homozygous	116669660
10	87348374	87348375	G	A	32	GENIC	homozygous	116949594
10	87348591	87348592	C	T	18	GENIC	homozygous	116949596
10	87348721	87348722	A	T	24	GENIC	homozygous	116949598
10	87348911	87348912	G	C	33	GENIC	homozygous	116949600
10	87349485	87349486	C	T	22	GENIC	homozygous	116949602
10	87349490	87349491	T	G	22	GENIC	homozygous	116949604