chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117457980	117457981	A	G	20	GENIC	homozygous	117124825
8	117459094	117459095	T	C	17	GENIC	homozygous	117124833
8	117460884	117460885	C	T	26	GENIC	homozygous	117124851
8	117462087	117462088	A	G	24	GENIC	possibly homozygous	117124859
8	117462354	117462355	C	T	18	GENIC	homozygous	116671506
8	117462477	117462478	A	G	15	GENIC	homozygous	117149505
8	117462488	117462489	A	G	15	GENIC	homozygous	117149506
8	117462614	117462615	C	T	11	GENIC	homozygous	117149507
8	117462629	117462630	A	G	9	GENIC	homozygous	117149508
8	117462692	117462693	C	T	21	GENIC	homozygous	117149509
8	117463605	117463606	C	T	23	GENIC	homozygous	117149511
8	117463853	117463854	C	T	24	GENIC	homozygous	117149512
8	117464433	117464434	G	A	10	GENIC	homozygous	117149514
8	117464601	117464602	T	C	26	GENIC	homozygous	116671516
8	117465468	117465469	G	T	25	GENIC	homozygous	117149515
8	117466249	117466250	A	C	27	GENIC	homozygous	116671520
8	117466294	117466295	T	C	30	GENIC	homozygous	117149516
8	117466327	117466328	C	A	29	GENIC	possibly homozygous	117149517
8	117466724	117466725	A	G	34	GENIC	homozygous	117149518
8	117466759	117466760	C	T	27	GENIC	homozygous	117149519
8	117466987	117466988	C	T	26	GENIC	homozygous	117149520
8	117467476	117467477	T	G	17	GENIC	homozygous	116671526
8	117469362	117469363	T	C	31	GENIC	homozygous	116671536
8	117470014	117470015	T	C	22	GENIC	homozygous	116671538
8	117471283	117471284	T	C	36	GENIC	homozygous	116671542
8	117471357	117471358	A	T	34	GENIC	homozygous	116671544
8	117475110	117475111	C	A	29	GENIC	homozygous	116671590