chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	250468571	250468572	A	C	16	GENIC	homozygous	108607968
1	250468684	250468685	C	T	7	GENIC	homozygous	108607970
1	250468688	250468689	A	T	6	GENIC	homozygous	108607971
1	250468692	250468693	A	T	6	GENIC	homozygous	108607972
1	250468697	250468698	C	G	6	GENIC	homozygous	108607974
1	250468701	250468702	C	A	4	GENIC	homozygous	108607975
1	250468702	250468703	C	A	4	GENIC	homozygous	108607977
1	250468706	250468707	C	A	4	GENIC	homozygous	108607978
1	250468748	250468749	C	T	11	GENIC	homozygous	108607980
1	250468762	250468763	C	G	10	GENIC	homozygous	108607982
1	250472094	250472095	G	T	6	GENIC	homozygous	108778140
1	250472194	250472195	A	T	4	GENIC	homozygous	108607983
1	250493769	250493770	A	T	28	GENIC	possibly homozygous	108778144
1	250500915	250500916	C	G	19	GENIC	possibly homozygous	108608096
1	250500990	250500991	A	T	18	GENIC	homozygous	108608098
1	250501197	250501198	T	C	41	GENIC	heterozygous	108608100
1	250501203	250501204	C	T	44	GENIC	heterozygous	108608102
1	250501221	250501222	C	A	40	GENIC	heterozygous	108608103
1	250501225	250501226	A	T	40	GENIC	heterozygous	108608105
1	250501229	250501230	G	A	41	GENIC	heterozygous	108608106
1	250502946	250502947	G	T	16	GENIC	homozygous	108608110
1	250503567	250503568	T	G	2	GENIC	homozygous	108608112
1	250504148	250504149	C	G	5	GENIC	homozygous	108608117
1	250511588	250511589	C	G	4	GENIC	homozygous	108608119