chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	256745437	256745438	C	G	39	GENIC	homozygous	108622645
1	256748087	256748088	A	G	56	GENIC	homozygous	108622653
1	256748605	256748606	T	C	53	GENIC	possibly homozygous	109024008
1	256749952	256749953	G	T	38	GENIC	homozygous	109024009
1	256751347	256751348	T	C	54	GENIC	possibly homozygous	109024010
1	256752387	256752388	G	A	48	GENIC	homozygous	109024011
1	256753404	256753405	G	A	20	GENIC	possibly homozygous	109024012
1	256754372	256754373	G	A	59	GENIC	homozygous	109024013
1	256755907	256755908	A	G	63	GENIC	homozygous	108622656
1	256756423	256756424	G	T	61	GENIC	homozygous	108622657
1	256757119	256757120	G	C	42	GENIC	homozygous	109024016
1	256757140	256757141	G	A	48	GENIC	homozygous	109024017
1	256757188	256757189	C	T	46	GENIC	possibly homozygous	109024018
1	256757814	256757815	T	C	57	GENIC	homozygous	108622659
1	256758532	256758533	A	G	42	GENIC	homozygous	108622660
1	256759132	256759133	G	A	28	GENIC	possibly homozygous	108622663
1	256760176	256760177	A	G	52	GENIC	homozygous	108622664
1	256760256	256760257	A	G	58	GENIC	homozygous	108622666
1	256760295	256760296	A	G	48	GENIC	homozygous	109024021
1	256760627	256760628	A	G	40	GENIC	homozygous	109214963
1	256755979	256755980	C	G	59	GENIC	homozygous	109214959
1	256759980	256759981	C	T	52	GENIC	homozygous	109214961
1	256760454	256760455	G	A	51	GENIC	homozygous	108622667