chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10696027	10696028	A	G	35	GENIC	homozygous	138513691
9	10696427	10696428	G	T	24	GENIC	homozygous	138513692
9	10697809	10697810	C	T	15	GENIC	homozygous	138513693
9	10698829	10698830	A	T	14	GENIC	homozygous	138513694
9	10700706	10700707	T	A	31	GENIC	possibly homozygous	138513695
9	10701592	10701593	T	C	16	GENIC	homozygous	138513696
9	10704254	10704255	G	C	15	GENIC	homozygous	138513697
9	10705043	10705044	C	A	24	GENIC	homozygous	138513698
9	10705107	10705108	C	A	28	GENIC	homozygous	138513699
9	10699194	10699194		GTTATTTAA	13	GENIC	homozygous	138446567
9	10707096	10707097	G	A	20	GENIC	homozygous	138513700
9	10708601	10708602	A	T	16	GENIC	homozygous	138513701
9	10709630	10709631	A	G	19	GENIC	homozygous	138513702
9	10709646	10709647	G	A	17	GENIC	homozygous	138513703
9	10710813	10710814	T	C	22	GENIC	homozygous	138513704
9	10712380	10712381	T	C	23	GENIC	homozygous	138513705