chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94287350	94287351	C	G	33	GENIC	homozygous	53600086
9	94287568	94287569	G	A	28	GENIC	homozygous	53600087
9	94287761	94287762	G	A	34	GENIC	homozygous	53600088
9	94287891	94287892	T	G	23	GENIC	homozygous	53600089
9	94288100	94288101	A	G	35	GENIC	homozygous	52280430
9	94288221	94288222	T	C	15	GENIC	homozygous	52052706
9	94288439	94288440	T	G	29	GENIC	homozygous	52052708
9	94289135	94289136	G	A	32	GENIC	homozygous	52052710
9	94289520	94289521	G	-	17	GENIC	homozygous	52052712
9	94290179	94290180	T	TAGGCCTGTTCTGGGTCAGGCACAGCAGGACATGCCTGCAATGCCAGTACTTAGGAGGCTGAGGTGGGACTGGGAGTTTAAGGCCAATCTGG	44	INTERGENIC	homozygous	52861468
9	94290424	94290425	A	G	25	INTERGENIC	homozygous	52052714
9	94290633	94290634	G	A	33	INTERGENIC	homozygous	52052716
9	94291689	94291691	GG	--	16	GENIC	homozygous	52861470
9	94291694	94291695	G	T	19	GENIC	homozygous	52861472
9	94292527	94292528	G	GT	26	GENIC	homozygous	52052722
9	94292529	94292530	C	A	26	GENIC	homozygous	52861474
9	94292702	94292703	A	G	28	GENIC	homozygous	52052724
9	94293221	94293222	G	A	28	GENIC	homozygous	52052726
9	94293996	94293997	G	A	26	GENIC	homozygous	53600090
9	94294200	94294201	T	C	38	GENIC	homozygous	52052730