chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15393827	15393828	C	G	40	GENIC	possibly homozygous	117680392
9	15393831	15393832	C	G	39	GENIC	possibly homozygous	117680393
9	15394058	15394059	T	C	48	GENIC	homozygous	117680394
9	15394100	15394101	G	C	43	GENIC	homozygous	117680395
9	15395044	15395045	A	T	67	GENIC	possibly homozygous	117680396
9	15395292	15395293	A	G	48	GENIC	homozygous	117267719
9	15396097	15396098	G	A	73	GENIC	homozygous	117680397
9	15398021	15398022	T	A	42	GENIC	homozygous	117680398
9	15399028	15399029	A	C	63	GENIC	homozygous	117267727
9	15399987	15399988	G	T	37	GENIC	possibly homozygous	117267730
9	15400996	15400997	C	A	62	GENIC	homozygous	117680399
9	15402684	15402685	C	T	79	GENIC	possibly homozygous	117680400
9	15402716	15402717	G	A	75	GENIC	homozygous	117680401
9	15394714	15394714		TG	45	GENIC	homozygous	132132521
9	15401351	15401360	CCATGGGCA		69	GENIC	homozygous	131063747