chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102110896	102110897	C	CG	16	GENIC	homozygous	60779935
1	102110898	102110899	G	GCT	13	GENIC	homozygous	60779936
1	102111238	102111239	T	C	15	GENIC	homozygous	60779937
1	102111319	102111320	G	GC	11	INTERGENIC	homozygous	61299558
1	102111446	102111447	T	-	1	INTERGENIC	homozygous	61299559
1	102129096	102129097	T	TG	25	GENIC	homozygous	60779938
1	102130969	102130970	T	C	19	GENIC	heterozygous	61485904
1	102139605	102139606	G	GA	17	INTERGENIC	homozygous	60779940
1	102139622	102139623	T	TGA	15	INTERGENIC	homozygous	60779941
1	102140718	102140720	GG	--	7	INTERGENIC	heterozygous	60779943
1	102143296	102143297	T	C	19	GENIC	heterozygous	60779945
1	102143316	102143317	A	G	24	GENIC	possibly homozygous	60779946
1	102144992	102144993	G	A	22	GENIC	heterozygous	60779947
1	102144996	102144997	G	A	21	GENIC	heterozygous	60779948
1	102145026	102145027	G	A	17	GENIC	heterozygous	61732224
1	102149772	102149773	G	GCTTGC	1	GENIC	homozygous	61299563
1	102157290	102157291	T	-	16	GENIC	heterozygous	61485921
1	102163408	102163409	G	A	24	INTERGENIC	heterozygous	61485935
1	102174376	102174377	T	-	16	INTERGENIC	homozygous	60779956
1	102175552	102175553	G	GC	24	INTERGENIC	homozygous	60779957
1	102185292	102185293	G	-	28	INTERGENIC	heterozygous	60779958