chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	173939816	173939816		A	53	GENIC	homozygous	135961021
2	173940445	173940445		T	53	GENIC	possibly homozygous	135961022
2	173941915	173941916	A	G	60	GENIC	homozygous	136372588
2	173942910	173942911	A	C	29	GENIC	possibly homozygous	403883252
2	173942909	173942910	A		29	GENIC	possibly homozygous	403562018
2	173942909	173942910	A	C	29	GENIC	heterozygous	403562019
2	173942910	173942911	A		29	GENIC	heterozygous	403883251
2	173942907	173942908	A		29	GENIC	possibly homozygous	403027858
2	173942907	173942908	A	C	29	GENIC	heterozygous	403027859
2	173943800	173943801	G		45	GENIC	homozygous	135961023
2	173944287	173944288	C		58	GENIC	homozygous	135961024
2	173948550	173948551	C	T	60	GENIC	homozygous	136372592
2	173952597	173952597		GA	19	GENIC	possibly homozygous	135961030
2	173954178	173954179	T	A	70	GENIC	homozygous	136372606
2	173948931	173948933	GC		56	GENIC	homozygous	141334163
2	173951622	173951622		T	52	GENIC	possibly homozygous	141334164
2	173950913	173950914	G	A	41	GENIC	homozygous	141422228
2	173956071	173956072	T		29	GENIC	homozygous	403027860
2	173956071	173956072	T	C	29	GENIC	heterozygous	403027861
2	173956073	173956074	T	C	29	GENIC	homozygous	141422229
2	173956827	173956828	C	T	45	GENIC	homozygous	141422230