chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89183036	89183037	G	A	14	INTERGENIC	homozygous	51536742
10	89183676	89183677	T	C	9	INTERGENIC	homozygous	51536743
10	89184172	89184173	T	C	7	INTERGENIC	possibly homozygous	51536744
10	89186321	89186322	A	T	15	INTERGENIC	homozygous	51536746
10	89188780	89188781	C	CG	18	INTERGENIC	possibly homozygous	51536761
10	89189903	89189904	C	T	8	INTERGENIC	homozygous	51536762
10	89190716	89190717	A	AT	2	INTERGENIC	heterozygous	51536765
10	89191497	89191498	C	T	19	INTERGENIC	possibly homozygous	51536766
10	89191702	89191703	C	T	30	INTERGENIC	homozygous	51536767
10	89192676	89192677	G	A	20	GENIC	possibly homozygous	51536768
10	89193666	89193667	A	G	20	GENIC	possibly homozygous	51536769
10	89194827	89194828	C	-	3	GENIC	heterozygous	51536770
10	89195084	89195085	A	G	14	GENIC	possibly homozygous	51536771
10	89198127	89198128	C	T	18	GENIC	homozygous	51536773
10	89198268	89198269	G	A	26	GENIC	homozygous	51536774