chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	267076083	267076084	C	T	45	GENIC	homozygous	108639140
1	267076179	267076180	A	C	35	GENIC	homozygous	108639141
1	267076233	267076234	G	A	38	GENIC	homozygous	109028646
1	267077197	267077198	A	G	55	GENIC	homozygous	108639142
1	267077292	267077293	A	G	38	GENIC	homozygous	108639143
1	267077781	267077782	T	G	53	GENIC	possibly homozygous	108639145
1	267078108	267078109	C	T	31	GENIC	homozygous	109028647
1	267078178	267078179	C	T	40	GENIC	homozygous	108639146
1	267078361	267078362	T	C	41	GENIC	homozygous	108639147
1	267079154	267079155	C	T	34	GENIC	possibly homozygous	109028648
1	267082313	267082314	C	T	39	GENIC	homozygous	109028650
1	267082500	267082501	A	G	25	GENIC	homozygous	108639151
1	267083326	267083327	A	G	39	GENIC	homozygous	108639153
1	267083376	267083377	G	A	32	GENIC	homozygous	109028651
1	267083423	267083424	G	A	32	GENIC	homozygous	109028652
1	267083561	267083562	T	C	48	GENIC	homozygous	108639154
1	267084220	267084221	C	T	41	GENIC	homozygous	108639156
1	267084444	267084445	G	A	26	GENIC	possibly homozygous	109028653
1	267084975	267084976	A	G	34	GENIC	possibly homozygous	108639160
1	267084995	267084996	A	G	31	GENIC	homozygous	108639161
1	267085759	267085760	T	C	30	GENIC	homozygous	108639163
1	267085781	267085782	C	T	32	GENIC	homozygous	109028654
1	267085850	267085851	A	G	37	GENIC	homozygous	108639164
1	267086128	267086129	T	A	28	GENIC	homozygous	108639165
1	267086561	267086562	G	A	32	GENIC	homozygous	109028655
1	267086726	267086727	G	A	31	GENIC	homozygous	109028656
1	267086866	267086867	T	C	39	GENIC	homozygous	108639167
1	267087407	267087408	A	G	37	GENIC	homozygous	108639168
1	267087875	267087876	A	G	27	GENIC	homozygous	109028657