chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	261324154	261324155	A	G	18	GENIC	homozygous	108629322
1	261325082	261325083	A	G	29	GENIC	homozygous	108629325
1	261325363	261325364	C	T	27	GENIC	homozygous	108629326
1	261326097	261326098	C	A	28	GENIC	homozygous	109025984
1	261326234	261326235	A	C	31	GENIC	possibly homozygous	109025985
1	261327227	261327228	T	C	31	GENIC	possibly homozygous	120881346
1	261327326	261327327	A	G	26	GENIC	homozygous	108629327
1	261327505	261327506	C	T	25	GENIC	possibly homozygous	109025986
1	261327960	261327961	T	G	39	GENIC	possibly homozygous	109025987
1	261328035	261328036	A	G	36	GENIC	homozygous	108629328
1	261328678	261328679	G	A	47	GENIC	possibly homozygous	109025989
1	261328887	261328888	G	A	48	GENIC	homozygous	108629334
1	261331197	261331198	C	T	23	GENIC	possibly homozygous	109025990
1	261332215	261332216	C	T	19	GENIC	possibly homozygous	109025991
1	261332233	261332234	C	T	28	GENIC	possibly homozygous	109025992
1	261332358	261332359	G	A	24	GENIC	homozygous	108629345
1	261332473	261332474	T	C	27	GENIC	homozygous	108629346
1	261332941	261332942	A	C	22	GENIC	homozygous	108629348