chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263505878	263505879	G	A	21	GENIC	homozygous	108633190
1	263505886	263505887	C	T	21	GENIC	homozygous	108633192
1	263505907	263505908	G	A	17	GENIC	homozygous	108633194
1	263505920	263505921	G	A	14	GENIC	homozygous	108633195
1	263505944	263505945	G	A	9	GENIC	homozygous	108633197
1	263506418	263506419	C	A	11	GENIC	homozygous	108633202
1	263506687	263506688	G	A	19	GENIC	homozygous	108633204
1	263506819	263506820	T	A	22	GENIC	homozygous	108633206
1	263506844	263506845	T	C	24	GENIC	homozygous	108633208
1	263506973	263506974	T	C	25	GENIC	homozygous	108633210
1	263507031	263507032	T	C	19	GENIC	homozygous	108633212
1	263507700	263507701	A	G	14	GENIC	homozygous	108633214
1	263507738	263507739	A	G	15	GENIC	homozygous	108633216
1	263507998	263507999	C	T	23	GENIC	homozygous	108633218
1	263508005	263508006	C	T	22	GENIC	homozygous	108633220
1	263508405	263508406	G	C	22	GENIC	homozygous	108633222
1	263508558	263508559	T	C	25	GENIC	homozygous	108633224
1	263509169	263509170	A	G	19	GENIC	homozygous	108633226
1	263509420	263509421	C	A	14	GENIC	homozygous	108633228
1	263509506	263509507	G	C	10	GENIC	homozygous	108633230
1	263509864	263509865	T	C	9	GENIC	homozygous	108633232
1	263509936	263509937	T	C	17	GENIC	homozygous	108633233
1	263509980	263509981	T	C	21	GENIC	homozygous	108633235
1	263510980	263510981	T	C	21	GENIC	homozygous	108633239
1	263511210	263511211	C	T	20	GENIC	homozygous	108633241