chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	51490373	51490374	C	G	24	GENIC	homozygous	61413057
1	51496499	51496500	G	A	42	GENIC	homozygous	61413058
1	51508975	51508976	A	-	11	GENIC	homozygous	61868225
1	51512774	51512775	G	C	22	GENIC	homozygous	61413064
1	51513870	51513874	TACA	----	20	GENIC	homozygous	61868226
1	51516113	51516114	T	C	23	GENIC	homozygous	61868227
1	51522101	51522102	A	AAC	6	GENIC	heterozygous	62127247
1	51522102	51522104	AC	--	6	GENIC	heterozygous	62226440
1	51526302	51526304	GT	--	6	GENIC	heterozygous	62226441
1	51533345	51533346	T	TGA	16	GENIC	heterozygous	62127248
1	51534678	51534679	A	-	10	GENIC	possibly homozygous	60699946
1	51536143	51536144	G	GA	10	GENIC	homozygous	61290608
1	51539482	51539484	AC	--	1	GENIC	homozygous	60699947
1	51543372	51543373	C	CA	5	GENIC	heterozygous	62226442
1	51543373	51543374	A	-	5	GENIC	heterozygous	60699948
1	51547263	51547264	T	C	28	GENIC	homozygous	61413068
1	51551879	51551880	A	G	33	GENIC	homozygous	61413069
1	51552088	51552089	C	G	31	GENIC	homozygous	60699950
1	51559566	51559567	A	-	9	GENIC	heterozygous	62226443
1	51572857	51572858	G	GA	17	GENIC	homozygous	61413071
1	51575452	51575453	T	TGG	9	GENIC	homozygous	61868232
1	51575661	51575662	A	G	17	GENIC	homozygous	61413072
1	51575800	51575801	G	GC	6	GENIC	homozygous	61666292
1	51575854	51575855	C	T	22	GENIC	homozygous	61413074
1	51576780	51576781	G	C	9	GENIC	homozygous	61868233