chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	146681229	146681230	C	T	32	GENIC	homozygous	56069740
5	146682774	146682775	G	A	30	GENIC	homozygous	56069741
5	146685033	146685034	A	AC	14	GENIC	possibly homozygous	56069742
5	146685174	146685175	T	C	13	GENIC	homozygous	55773387
5	146690319	146690320	G	A	19	GENIC	homozygous	56069743
5	146693020	146693021	C	T	37	GENIC	possibly homozygous	55773391
5	146693082	146693083	A	G	26	GENIC	possibly homozygous	56069744
5	146693339	146693340	T	C	28	GENIC	possibly homozygous	56069745
5	146693408	146693409	G	A	25	GENIC	homozygous	56069746
5	146694973	146694974	T	TAC	5	GENIC	homozygous	56589558
5	146695011	146695012	C	CACAT	10	GENIC	heterozygous	56069747
5	146695035	146695036	C	T	27	GENIC	homozygous	56069748
5	146695636	146695637	C	T	36	GENIC	homozygous	55773404
5	146695720	146695721	C	G	25	GENIC	homozygous	56069749
5	146696102	146696103	T	C	25	GENIC	homozygous	56069750
5	146696282	146696283	A	T	32	GENIC	homozygous	56069751
5	146696432	146696433	T	C	28	GENIC	homozygous	55773406
5	146696607	146696608	A	T	34	GENIC	possibly homozygous	56069752
5	146698033	146698035	CC	--	24	GENIC	homozygous	55773410
5	146699376	146699377	A	G	32	GENIC	homozygous	56069753
5	146699959	146699961	TT	--	25	GENIC	possibly homozygous	55773412
5	146699960	146699961	T	-	25	GENIC	heterozygous	55773414