chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	69651798	69651799	A	G	14	GENIC	homozygous	46746089
18	69652076	69652077	T	C	18	GENIC	homozygous	46746090
18	69652093	69652094	T	C	23	GENIC	homozygous	46746091
18	69654089	69654090	C	T	9	GENIC	homozygous	46746093
18	69655040	69655041	A	G	20	GENIC	homozygous	46746095
18	69655183	69655184	T	TG	14	GENIC	heterozygous	46799940
18	69655184	69655185	G	-	14	GENIC	possibly homozygous	46746096
18	69655476	69655477	G	A	17	GENIC	possibly homozygous	46746097
18	69655786	69655787	A	G	10	GENIC	homozygous	46746098
18	69656011	69656012	A	G	10	GENIC	homozygous	46746099
18	69656083	69656084	T	C	8	GENIC	homozygous	46746100
18	69656156	69656157	A	G	7	GENIC	possibly homozygous	46746101
18	69656308	69656309	C	G	17	GENIC	homozygous	46746102
18	69656623	69656624	A	G	14	GENIC	homozygous	46746103
18	69656853	69656854	A	G	10	GENIC	homozygous	46746104
18	69656944	69656945	G	A	21	GENIC	possibly homozygous	46746105