chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	94873709	94873710	G	GGTGT	13	GENIC	homozygous	53008238
8	94874414	94874415	C	CA	14	GENIC	homozygous	52741147
8	94874628	94874629	G	T	11	GENIC	heterozygous	53008239
8	94874665	94874666	G	-	11	GENIC	possibly homozygous	52741151
8	94874965	94874966	G	T	18	GENIC	homozygous	52741153
8	94875025	94875029	GTTC	----	6	GENIC	homozygous	52741154
8	94875033	94875036	TTT	---	9	GENIC	heterozygous	52741155
8	94876554	94876555	A	G	5	GENIC	heterozygous	52741170
8	94886772	94886773	G	T	29	GENIC	homozygous	53348059
8	94886812	94886813	C	G	29	GENIC	homozygous	53008261
8	94887270	94887271	C	T	27	GENIC	homozygous	53348061
8	94887509	94887510	T	A	30	GENIC	homozygous	52741222
8	94887522	94887523	T	G	33	GENIC	homozygous	52741223
8	94887891	94887892	C	T	32	GENIC	homozygous	53348062
8	94887939	94887940	T	C	32	GENIC	possibly homozygous	52741225