chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116083187	116083188	G	A	58	GENIC	homozygous	116668359
8	116083295	116083296	G	A	60	GENIC	homozygous	116668361
8	116083680	116083681	C	A	75	GENIC	homozygous	116668363
8	116084552	116084553	G	T	48	GENIC	possibly homozygous	116668365
8	116085385	116085386	A	G	48	GENIC	possibly homozygous	116668367
8	116085453	116085454	C	T	56	GENIC	homozygous	116668369
8	116085630	116085631	G	A	55	GENIC	homozygous	116668371
8	116085942	116085943	C	T	42	GENIC	possibly homozygous	116668373
8	116086576	116086577	G	T	45	GENIC	homozygous	116668375
8	116086854	116086855	C	T	34	GENIC	homozygous	116668377
8	116087089	116087090	T	C	52	GENIC	homozygous	116668379
8	116087510	116087511	T	C	62	GENIC	homozygous	116668381
8	116087721	116087722	A	G	50	GENIC	homozygous	116668383
8	116087816	116087817	T	C	46	GENIC	homozygous	116668385
8	116087918	116087919	A	G	56	GENIC	homozygous	116668387
8	116088288	116088289	C	T	50	GENIC	homozygous	116668389
8	116088428	116088429	G	C	43	GENIC	homozygous	116668391
8	116088429	116088430	A	C	43	GENIC	homozygous	116668393
8	116088488	116088489	C	T	45	GENIC	possibly homozygous	116668395
8	116088521	116088522	T	C	50	GENIC	homozygous	116668397
8	116088833	116088834	C	T	49	GENIC	homozygous	116668399
8	116088911	116088912	G	A	52	GENIC	homozygous	116668401
8	116089521	116089522	A	G	41	GENIC	homozygous	116668403
8	116089701	116089702	A	G	52	GENIC	homozygous	116668405
8	116089736	116089737	A	G	68	GENIC	possibly homozygous	116668407
8	116089788	116089789	C	G	70	GENIC	homozygous	116668409
8	116090259	116090260	T	C	52	GENIC	homozygous	116668411
8	116090433	116090434	A	T	60	GENIC	homozygous	116668413
8	116090580	116090581	T	C	65	GENIC	homozygous	116668415
8	116091424	116091425	G	C	48	GENIC	homozygous	116668417
8	116091790	116091791	A	G	51	GENIC	homozygous	116668419
8	116092563	116092564	G	A	48	GENIC	homozygous	116668421