chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116083680	116083681	C	A	47	GENIC	possibly homozygous	116668363
8	116083757	116083758	C	G	42	GENIC	homozygous	116987970
8	116084552	116084553	G	T	47	GENIC	heterozygous	116668365
8	116085385	116085386	A	G	38	GENIC	homozygous	116668367
8	116085453	116085454	C	T	47	GENIC	possibly homozygous	116668369
8	116086493	116086494	T	G	26	GENIC	possibly homozygous	116987971
8	116086576	116086577	G	T	42	GENIC	homozygous	116668375
8	116086854	116086855	C	T	37	GENIC	possibly homozygous	116668377
8	116087089	116087090	T	C	48	GENIC	homozygous	116668379
8	116087510	116087511	T	C	45	GENIC	homozygous	116668381
8	116087721	116087722	A	G	45	GENIC	homozygous	116668383
8	116087816	116087817	T	C	45	GENIC	homozygous	116668385
8	116087835	116087836	C	T	35	GENIC	possibly homozygous	116886009
8	116087918	116087919	A	G	53	GENIC	homozygous	116668387
8	116088428	116088429	G	C	25	GENIC	homozygous	116668391
8	116088429	116088430	A	C	24	GENIC	homozygous	116668393
8	116088521	116088522	T	C	31	GENIC	homozygous	116668397
8	116088911	116088912	G	A	41	GENIC	homozygous	116668401
8	116089521	116089522	A	G	54	GENIC	homozygous	116668403
8	116089701	116089702	A	G	65	GENIC	homozygous	116668405
8	116089736	116089737	A	G	62	GENIC	homozygous	116668407
8	116089788	116089789	C	G	54	GENIC	possibly homozygous	116668409
8	116090259	116090260	T	C	62	GENIC	homozygous	116668411
8	116090433	116090434	A	T	40	GENIC	homozygous	116668413
8	116090580	116090581	T	C	40	GENIC	homozygous	116668415
8	116090856	116090857	A	T	48	GENIC	homozygous	116886013
8	116091790	116091791	A	G	51	GENIC	homozygous	116668419
8	116092563	116092564	G	A	49	GENIC	homozygous	116668421
8	116092854	116092855	A	T	35	GENIC	heterozygous	116987972