chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	274339059	274339060	T	A	29	GENIC	homozygous	61226568
1	274339180	274339181	G	A	33	GENIC	homozygous	61647129
1	274339787	274339788	T	G	16	GENIC	homozygous	61647130
1	274339994	274339995	A	T	46	GENIC	homozygous	61647131
1	274340009	274340010	A	G	47	GENIC	homozygous	61226569
1	274340034	274340035	T	C	37	GENIC	homozygous	61226570
1	274340095	274340096	A	T	29	GENIC	homozygous	61647132
1	274340524	274340525	G	A	29	GENIC	homozygous	61647133
1	274341798	274341799	G	A	38	GENIC	homozygous	61647134
1	274342425	274342426	C	T	34	GENIC	homozygous	61647135
1	274342688	274342689	C	T	23	GENIC	homozygous	61647136
1	274342839	274342840	C	T	16	GENIC	homozygous	61226573
1	274342853	274342854	G	-	16	GENIC	homozygous	61647137
1	274342900	274342901	G	GAAAAAA	13	GENIC	homozygous	62559155
1	274343687	274343688	G	T	41	GENIC	possibly homozygous	61647138
1	274343693	274343694	T	TGG	37	GENIC	homozygous	61647139
1	274343709	274343710	C	CA	33	GENIC	homozygous	61647140
1	274344348	274344349	G	GCGC	28	GENIC	homozygous	61647141
1	274344439	274344440	A	G	46	GENIC	possibly homozygous	61647143