chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116083187	116083188	G	A	32	GENIC	homozygous	116668359
8	116083295	116083296	G	A	24	GENIC	homozygous	116668361
8	116083680	116083681	C	A	20	GENIC	homozygous	116668363
8	116084552	116084553	G	T	9	GENIC	heterozygous	116668365
8	116085385	116085386	A	G	23	GENIC	homozygous	116668367
8	116085453	116085454	C	T	20	GENIC	homozygous	116668369
8	116085630	116085631	G	A	13	GENIC	homozygous	116668371
8	116085942	116085943	C	T	9	GENIC	homozygous	116668373
8	116086576	116086577	G	T	17	GENIC	homozygous	116668375
8	116087510	116087511	T	C	14	GENIC	homozygous	116668381
8	116087721	116087722	A	G	16	GENIC	homozygous	116668383
8	116087816	116087817	T	C	7	GENIC	homozygous	116668385
8	116087918	116087919	A	G	19	GENIC	homozygous	116668387
8	116088288	116088289	C	T	16	GENIC	homozygous	116668389
8	116088428	116088429	G	C	11	GENIC	homozygous	116668391
8	116088429	116088430	A	C	9	GENIC	homozygous	116668393
8	116088488	116088489	C	T	19	GENIC	homozygous	116668395
8	116088521	116088522	T	C	27	GENIC	homozygous	116668397
8	116088833	116088834	C	T	8	GENIC	homozygous	116668399
8	116088911	116088912	G	A	23	GENIC	homozygous	116668401
8	116089521	116089522	A	G	18	GENIC	homozygous	116668403
8	116089701	116089702	A	G	14	GENIC	homozygous	116668405
8	116089736	116089737	A	G	5	GENIC	homozygous	116668407
8	116089788	116089789	C	G	14	GENIC	homozygous	116668409
8	116090259	116090260	T	C	32	GENIC	homozygous	116668411
8	116090433	116090434	A	T	22	GENIC	homozygous	116668413
8	116090580	116090581	T	C	29	GENIC	homozygous	116668415
8	116091424	116091425	G	C	25	GENIC	homozygous	116668417
8	116091790	116091791	A	G	19	GENIC	homozygous	116668419
8	116092563	116092564	G	A	27	GENIC	homozygous	116668421
8	116092854	116092855	A	T	19	GENIC	heterozygous	116987972