chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94291689	94291691	GG	--	14	GENIC	homozygous	52861470
9	94291694	94291695	G	T	15	GENIC	homozygous	52861472
9	94292527	94292528	G	GT	28	GENIC	homozygous	52052722
9	94292529	94292530	C	A	28	GENIC	homozygous	52861474
9	94292702	94292703	A	G	25	GENIC	homozygous	52052724
9	94293221	94293222	G	A	30	GENIC	homozygous	52052726
9	94294200	94294201	T	C	23	GENIC	homozygous	52052730
9	94295101	94295102	C	T	25	GENIC	homozygous	52280434
9	94295180	94295181	C	CGT	19	GENIC	heterozygous	52052732
9	94295316	94295317	A	ATG	41	GENIC	homozygous	52052740
9	94297292	94297293	G	GA	21	GENIC	homozygous	52052746
9	94297951	94297952	A	G	23	GENIC	homozygous	52052748
9	94299084	94299085	T	G	27	GENIC	homozygous	52052750
9	94299368	94299369	A	G	33	GENIC	homozygous	52052752
9	94299485	94299486	G	T	26	GENIC	homozygous	52280435
9	94299805	94299806	C	T	24	GENIC	homozygous	52280437
9	94299921	94299922	T	C	28	GENIC	homozygous	52052754
9	94299984	94299985	G	A	24	GENIC	homozygous	52052756
9	94300475	94300476	T	TCCCCTCCCCC	1	GENIC	homozygous	52915542
9	94320415	94320416	C	T	15	GENIC	homozygous	52052760
9	94322482	94322483	G	GT	10	GENIC	possibly homozygous	52915543
9	94322491	94322492	G	-	10	GENIC	homozygous	52052766