chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	61469233	61469234	A	G	19	GENIC	possibly homozygous	46483926
18	61469877	61469878	T	C	13	GENIC	homozygous	46483936
18	61470957	61470958	T	C	12	GENIC	homozygous	46483958
18	61470963	61470964	A	G	10	GENIC	homozygous	46483959
18	61470986	61470987	T	C	8	GENIC	homozygous	46483960
18	61471052	61471053	T	C	7	GENIC	homozygous	46483961
18	61471084	61471085	G	A	13	GENIC	homozygous	46741084
18	61471198	61471199	C	CAT	17	GENIC	possibly homozygous	46483962
18	61471221	61471222	G	C	19	GENIC	homozygous	46483963
18	61471256	61471257	A	G	23	GENIC	possibly homozygous	46741085
18	61471440	61471441	G	A	22	GENIC	homozygous	46741086
18	61471496	61471497	C	T	18	GENIC	homozygous	46483964
18	61471558	61471559	C	T	21	GENIC	possibly homozygous	46741088
18	61471720	61471721	A	G	29	GENIC	possibly homozygous	46741089
18	61471770	61471771	A	T	21	GENIC	possibly homozygous	46483965
18	61471934	61471935	G	A	14	GENIC	homozygous	46741090
18	61472103	61472104	G	T	7	GENIC	possibly homozygous	46741091
18	61472146	61472147	T	C	13	GENIC	possibly homozygous	46741092
18	61472253	61472254	T	C	17	GENIC	homozygous	46741093
18	61472326	61472327	A	G	3	GENIC	homozygous	46741094
18	61472333	61472334	T	A	2	GENIC	homozygous	46797731
18	61472334	61472335	G	T	2	GENIC	homozygous	46797733
18	61477103	61477104	T	A	2	GENIC	homozygous	46741095
18	61477112	61477113	A	G	6	GENIC	homozygous	46741096
18	61477273	61477274	T	A	13	GENIC	homozygous	46483979
18	61477419	61477420	G	A	9	GENIC	possibly homozygous	46741097
18	61477432	61477433	C	T	6	GENIC	homozygous	46741098
18	61477436	61477437	A	G	7	GENIC	homozygous	46483980
18	61477462	61477463	T	C	8	GENIC	heterozygous	46483981