chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	9690552	9690553	C	T	25	GENIC	homozygous	126605756
9	9690620	9690621	C	G	21	GENIC	homozygous	126605757
9	9691512	9691513	G	A	7	GENIC	homozygous	126605758
9	9691658	9691659	G	T	17	GENIC	homozygous	126605759
9	9691921	9691922	C	T	16	GENIC	homozygous	126605760
9	9692591	9692592	T	C	14	GENIC	homozygous	126495989
9	9692750	9692751	A	C	17	GENIC	homozygous	126495990
9	9692837	9692838	A	T	7	GENIC	homozygous	126495991
9	9693105	9693106	G	A	12	GENIC	homozygous	126495992
9	9694643	9694644	T	C	17	GENIC	homozygous	126495998
9	9695313	9695314	A	G	8	GENIC	homozygous	126496000
9	9695470	9695471	A	G	18	GENIC	homozygous	126496001
9	9696066	9696067	T	C	7	GENIC	heterozygous	126496002
9	9696067	9696068	T	C	7	GENIC	homozygous	126496003
9	9698244	9698245	T	C	19	GENIC	homozygous	126496006
9	9698322	9698323	T	C	19	GENIC	homozygous	126496007
9	9698939	9698940	G	A	18	GENIC	homozygous	126605761
9	9699148	9699149	G	C	3	GENIC	heterozygous	126605762
9	9699565	9699566	G	A	28	GENIC	homozygous	126605763
9	9699785	9699786	T	C	10	GENIC	homozygous	126496009
9	9700261	9700262	A	T	6	GENIC	homozygous	126605764
9	9700592	9700593	C	T	16	GENIC	homozygous	126605765
9	9700739	9700740	C	A	18	GENIC	homozygous	126605766
9	9700832	9700833	A	G	7	GENIC	homozygous	126605767
9	9701137	9701138	A	G	16	GENIC	homozygous	126605768