chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	9761525	9761526	G	A	12	GENIC	homozygous	117243573
9	9762120	9762121	A	G	16	GENIC	homozygous	117243574
9	9762235	9762236	C	T	18	GENIC	homozygous	117243575
9	9762260	9762261	G	A	17	GENIC	homozygous	117243576
9	9762361	9762361		TTAG	12	GENIC	homozygous	128678049
9	9762654	9762655	A	G	17	GENIC	homozygous	117243577
9	9762867	9762868	G	A	19	GENIC	homozygous	117243578
9	9762876	9762877	G	A	17	GENIC	homozygous	117243579
9	9763123	9763124	G	T	13	GENIC	homozygous	117243580
9	9763204	9763205	A	C	14	GENIC	homozygous	117243581
9	9763554	9763555	C	G	8	GENIC	homozygous	117243582
9	9763599	9763600	C	T	7	GENIC	homozygous	117243583
9	9763789	9763790	A	G	12	GENIC	homozygous	117243584
9	9763884	9763884		A	10	GENIC	homozygous	128678050
9	9764910	9764911	T	C	11	GENIC	homozygous	117243588
9	9764071	9764072	A	G	14	GENIC	homozygous	117243585
9	9764187	9764188	C	T	13	GENIC	homozygous	117243586
9	9764188	9764189	A	G	13	GENIC	homozygous	117243587