chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116440435	116440436	A	G	29	GENIC	homozygous	116669365
8	116442167	116442168	G	A	26	GENIC	homozygous	116988081
8	116445025	116445026	C	T	27	GENIC	homozygous	116988082
8	116445837	116445838	A	T	24	GENIC	homozygous	116988083
8	116447898	116447899	T	C	29	GENIC	homozygous	116669375
8	116452145	116452146	G	A	31	GENIC	homozygous	116988084
8	116455245	116455246	G	A	28	GENIC	homozygous	116669383
8	116456152	116456153	A	T	15	GENIC	homozygous	116886475
8	116456155	116456156	T	A	17	GENIC	homozygous	116988085
8	116457515	116457516	C	T	40	GENIC	homozygous	116886479
8	116457555	116457556	G	C	35	GENIC	homozygous	116988086
8	116460232	116460233	A	G	33	GENIC	homozygous	116988089
8	116460459	116460460	G	T	20	GENIC	homozygous	116988090
8	116460661	116460662	T	C	27	GENIC	homozygous	116886493
8	116460716	116460717	C	T	23	GENIC	homozygous	116886495
8	116460860	116460861	C	G	36	GENIC	homozygous	116886497
8	116461203	116461204	T	G	28	GENIC	homozygous	116886499
8	116461338	116461339	T	A	27	GENIC	homozygous	117920113
8	116461784	116461785	A	G	31	GENIC	homozygous	116669391
8	116462564	116462565	G	C	32	GENIC	homozygous	116988091
8	116463170	116463171	T	G	22	GENIC	homozygous	116988092
8	116463353	116463354	C	T	32	GENIC	homozygous	116886501
8	116464151	116464152	T	C	28	GENIC	homozygous	116669399
8	116465370	116465371	T	C	28	GENIC	homozygous	116669401