chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94291689	94291691	GG	--	33	GENIC	homozygous	52861470
9	94291694	94291695	G	T	33	GENIC	homozygous	52861472
9	94291762	94291763	C	T	35	GENIC	homozygous	52052720
9	94292527	94292528	G	GT	48	GENIC	homozygous	52052722
9	94292529	94292530	C	A	49	GENIC	homozygous	52861474
9	94292702	94292703	A	G	31	GENIC	homozygous	52052724
9	94293221	94293222	G	A	37	GENIC	homozygous	52052726
9	94293804	94293805	G	A	45	GENIC	homozygous	52052728
9	94294200	94294201	T	C	49	GENIC	homozygous	52052730
9	94295189	94295193	GTGT	----	17	GENIC	possibly homozygous	53238387
9	94296023	94296024	C	T	44	GENIC	homozygous	52052742
9	94296708	94296709	G	A	27	GENIC	homozygous	52052744
9	94297292	94297293	G	GA	28	GENIC	homozygous	52052746
9	94297951	94297952	A	G	33	GENIC	homozygous	52052748
9	94299084	94299085	T	G	38	GENIC	homozygous	52052750
9	94299368	94299369	A	G	60	GENIC	homozygous	52052752
9	94299921	94299922	T	C	33	GENIC	homozygous	52052754
9	94299984	94299985	G	A	25	GENIC	homozygous	52052756
9	94299991	94299992	C	CG	22	GENIC	homozygous	52052758
9	94300467	94300468	C	CTCTCTCTCTT	4	GENIC	heterozygous	53048167
9	94300475	94300476	T	TCCCCTCCCCC	4	GENIC	heterozygous	52915542
9	94320415	94320416	C	T	31	GENIC	homozygous	52052760
9	94322483	94322484	G	GT	13	GENIC	homozygous	52052762
9	94322491	94322492	G	-	13	GENIC	homozygous	52052766