chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	105568885	105568886	G	GA	26	GENIC	possibly homozygous	56048674
5	105569057	105569058	T	C	25	GENIC	homozygous	55618881
5	105569829	105569830	G	GA	18	GENIC	homozygous	56048675
5	105570089	105570090	T	C	16	GENIC	homozygous	56048676
5	105571248	105571249	A	G	33	GENIC	homozygous	55618883
5	105571985	105571986	T	TA	27	GENIC	homozygous	56048677
5	105574414	105574415	A	-	12	GENIC	possibly homozygous	56048678
5	105577938	105577939	C	CG	26	GENIC	homozygous	55618887
5	105581002	105581003	A	-	21	GENIC	homozygous	56120219
5	105582313	105582324	ATGCAAAAAAT	-----------	27	GENIC	homozygous	56048679
5	105586259	105586260	G	A	16	GENIC	homozygous	56048680
5	105586945	105586949	TCAG	----	21	GENIC	homozygous	55618892
5	105587021	105587023	AA	--	9	GENIC	homozygous	56441062
5	105588219	105588220	G	GT	19	GENIC	homozygous	55618895
5	105588790	105588791	T	TA	14	GENIC	heterozygous	56441064
5	105588996	105588998	AA	--	5	GENIC	homozygous	56579506
5	105589114	105589115	A	-	12	GENIC	heterozygous	56441068
5	105591315	105591316	A	T	23	GENIC	homozygous	56048683
5	105595788	105595789	A	-	2	GENIC	heterozygous	56441074
5	105597132	105597133	T	A	23	GENIC	possibly homozygous	56048684
5	105597849	105597850	C	CAA	9	GENIC	homozygous	56441080
5	105599976	105599978	TC	--	16	GENIC	homozygous	55618909