chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	24663100	24663101	T	C	14	GENIC	possibly homozygous	47351022
16	24663490	24663491	C	T	19	GENIC	homozygous	47351023
16	24663915	24663916	A	G	22	GENIC	homozygous	47351024
16	24664020	24664021	T	C	12	GENIC	homozygous	47351025
16	24664183	24664184	C	G	9	GENIC	homozygous	47351030
16	24664753	24664754	T	C	24	GENIC	possibly homozygous	47351031
16	24664788	24664789	C	T	14	GENIC	homozygous	47351032
16	24665112	24665113	T	G	28	GENIC	homozygous	47351033
16	24665548	24665549	A	G	13	GENIC	homozygous	47351034
16	24665633	24665634	T	C	15	GENIC	homozygous	47351035
16	24665843	24665844	A	C	5	GENIC	homozygous	47905614
16	24666293	24666294	C	G	26	GENIC	possibly homozygous	47630603
16	24666378	24666379	T	G	2	GENIC	homozygous	47630605
16	24667106	24667107	A	G	13	GENIC	homozygous	47351041
16	24667957	24667958	A	T	5	GENIC	homozygous	47905615
16	24667958	24667959	T	C	4	GENIC	homozygous	47905616
16	24668215	24668216	A	G	11	GENIC	homozygous	47351043
16	24668419	24668420	A	AG	7	GENIC	possibly homozygous	47351044
16	24668762	24668763	A	-	17	GENIC	homozygous	47351045