chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	146681229	146681230	C	T	25	GENIC	possibly homozygous	56069740
5	146682774	146682775	G	A	20	GENIC	possibly homozygous	56069741
5	146685174	146685175	T	C	2	GENIC	homozygous	55773387
5	146690319	146690320	G	A	25	GENIC	possibly homozygous	56069743
5	146693020	146693021	C	T	16	GENIC	homozygous	55773391
5	146693082	146693083	A	G	21	GENIC	possibly homozygous	56069744
5	146693339	146693340	T	C	24	GENIC	possibly homozygous	56069745
5	146693408	146693409	G	A	20	GENIC	possibly homozygous	56069746
5	146695035	146695036	C	T	18	GENIC	possibly homozygous	56069748
5	146695636	146695637	C	T	20	GENIC	homozygous	55773404
5	146695720	146695721	C	G	15	GENIC	homozygous	56069749
5	146696102	146696103	T	C	23	GENIC	possibly homozygous	56069750
5	146696282	146696283	A	T	22	GENIC	possibly homozygous	56069751
5	146696432	146696433	T	C	24	GENIC	homozygous	55773406
5	146696607	146696608	A	T	8	GENIC	homozygous	56069752
5	146698033	146698035	CC	--	19	GENIC	possibly homozygous	55773410
5	146699376	146699377	A	G	25	GENIC	homozygous	56069753