chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	9987988	9987989	C	G	7	GENIC	homozygous	128763333
9	9987991	9987991		A	7	GENIC	homozygous	128678551
9	9988002	9988002		AGGGGGA	6	GENIC	homozygous	128678552
9	9988007	9988007		AAA	6	GENIC	homozygous	128678553
9	9988008	9988008		C	5	GENIC	homozygous	128678554
9	9988016	9988017	C	A	7	GENIC	homozygous	117482566
9	9988019	9988019		C	7	GENIC	homozygous	128678555
9	9988032	9988033	G	C	19	GENIC	homozygous	117482568
9	9988035	9988035		C	19	GENIC	homozygous	128678556
9	9988234	9988235	G	A	58	GENIC	homozygous	117243914
9	9988428	9988429	G	A	38	GENIC	homozygous	117243915
9	9989377	9989378	C	T	36	GENIC	homozygous	117243916
9	9989996	9989997	G	A	49	GENIC	homozygous	117243917
9	9990842	9990843	T	C	32	GENIC	homozygous	117243918
9	9990855	9990856	G	A	32	GENIC	homozygous	117243919
9	9991856	9991857	C	T	48	GENIC	homozygous	117243920
9	9993554	9993555	A	G	53	GENIC	possibly homozygous	117243921
9	9993558	9993559	T	C	52	GENIC	possibly homozygous	117243922
9	9994038	9994039	G	A	44	GENIC	homozygous	117243923
9	9995515	9995516	G	A	43	GENIC	homozygous	117243924
9	9995927	9995928	T	C	33	GENIC	homozygous	117243925
9	9996938	9996939	T	C	33	GENIC	possibly homozygous	117243926
9	9997774	9997775	A		42	GENIC	possibly homozygous	128678557
9	9998188	9998189	T	C	44	GENIC	homozygous	117243927
9	9999789	9999790	C		38	GENIC	homozygous	128678558
9	9999792	9999803	TCCTTCCTTCC		38	GENIC	homozygous	128678559
9	10000558	10000559	C	T	37	GENIC	homozygous	117243930
9	10001276	10001277	C	A	61	GENIC	homozygous	117243931
9	10001372	10001372		TTTTC	38	GENIC	possibly homozygous	128678560
9	10001498	10001499	A	T	36	GENIC	homozygous	117243932
9	10002274	10002275	G	C	60	GENIC	homozygous	117243933