chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	256806534	256806535	C	G	14	GENIC	possibly homozygous	61170125
1	256806581	256806582	T	C	28	GENIC	possibly homozygous	61170126
1	256806885	256806886	C	T	21	GENIC	possibly homozygous	62634799
1	256807468	256807469	A	G	14	GENIC	possibly homozygous	61170127
1	256807866	256807867	C	T	18	GENIC	homozygous	61170128
1	256808595	256808596	G	A	12	GENIC	homozygous	61170129
1	256808686	256808687	C	A	15	GENIC	possibly homozygous	62634800
1	256809004	256809005	C	T	17	GENIC	possibly homozygous	62634801
1	256809495	256809496	G	GA	2	GENIC	homozygous	61170130
1	256811297	256811298	T	G	7	GENIC	homozygous	62634802
1	256811389	256811390	A	C	27	GENIC	homozygous	61170132
1	256811423	256811424	T	C	18	GENIC	homozygous	62634803
1	256811561	256811562	A	G	18	GENIC	possibly homozygous	62634804
1	256812128	256812129	C	T	3	GENIC	homozygous	62634805
1	256812192	256812193	A	-	11	GENIC	homozygous	62634806
1	256812638	256812639	C	-	2	GENIC	homozygous	62277160
1	256812640	256812643	CAT	---	3	GENIC	homozygous	62277161
1	256813113	256813114	C	A	15	GENIC	possibly homozygous	61170141
1	256813409	256813410	A	G	6	GENIC	homozygous	61170142