chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102110896	102110897	C	CG	31	GENIC	homozygous	60779935
1	102110898	102110899	G	GCT	28	GENIC	homozygous	60779936
1	102111238	102111239	T	C	29	GENIC	homozygous	60779937
1	102111319	102111320	G	GC	14	INTERGENIC	homozygous	61299558
1	102111446	102111447	T	-	2	INTERGENIC	homozygous	61299559
1	102113444	102113445	C	CT	47	GENIC	heterozygous	61299560
1	102129096	102129097	T	TG	43	GENIC	homozygous	60779938
1	102139605	102139606	G	GA	21	INTERGENIC	homozygous	60779940
1	102139622	102139623	T	TGA	11	INTERGENIC	homozygous	60779941
1	102140720	102140722	CA	--	15	INTERGENIC	heterozygous	61299561
1	102143061	102143062	T	-	19	GENIC	heterozygous	60779944
1	102143085	102143086	C	T	42	GENIC	heterozygous	61299562
1	102143296	102143297	T	C	37	GENIC	heterozygous	60779945
1	102143316	102143317	A	G	36	GENIC	heterozygous	60779946
1	102144992	102144993	G	A	35	GENIC	heterozygous	60779947
1	102144996	102144997	G	A	35	GENIC	heterozygous	60779948
1	102149772	102149773	G	GCTTGC	2	GENIC	homozygous	61299563
1	102152827	102152828	A	-	26	GENIC	possibly homozygous	60779950
1	102174376	102174377	T	-	27	INTERGENIC	possibly homozygous	60779956
1	102175552	102175553	G	GC	28	INTERGENIC	homozygous	60779957
1	102185292	102185293	G	-	28	INTERGENIC	heterozygous	60779958