chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94286603	94286604	G	C	27	GENIC	homozygous	52052702
9	94287501	94287502	G	A	30	GENIC	possibly homozygous	52280429
9	94288100	94288101	A	G	24	GENIC	homozygous	52280430
9	94288221	94288222	T	C	16	GENIC	homozygous	52052706
9	94288439	94288440	T	G	25	GENIC	homozygous	52052708
9	94289135	94289136	G	A	23	GENIC	homozygous	52052710
9	94289172	94289173	G	T	13	GENIC	homozygous	52280432
9	94289520	94289521	G	-	6	GENIC	homozygous	52052712
9	94290179	94290180	T	TAGGCCTGTTCTGGGTCAGGCACAGCAGGACATGCCTGCAATGCCAGTACTTAGGAGGCTGAGGTGGGACTGGGAGTTTAAGGCCAATCTGG	31	INTERGENIC	homozygous	52861468
9	94290424	94290425	A	G	21	INTERGENIC	homozygous	52052714
9	94290633	94290634	G	A	13	INTERGENIC	homozygous	52052716
9	94291689	94291691	GG	--	20	GENIC	homozygous	52861470
9	94291694	94291695	G	T	22	GENIC	homozygous	52861472
9	94292527	94292528	G	GT	34	GENIC	homozygous	52052722
9	94292529	94292530	C	A	34	GENIC	homozygous	52861474
9	94292702	94292703	A	G	13	GENIC	homozygous	52052724
9	94293221	94293222	G	A	20	GENIC	homozygous	52052726
9	94294200	94294201	T	C	23	GENIC	homozygous	52052730