chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94446140	94446141	A	AAAAG	7	GENIC	homozygous	51747159
10	94446424	94446425	A	G	26	GENIC	homozygous	51548898
10	94447117	94447118	T	C	39	GENIC	homozygous	51548899
10	94447208	94447209	A	G	35	GENIC	homozygous	51548900
10	94448512	94448513	A	G	20	GENIC	possibly homozygous	51747161
10	94448538	94448539	A	AC	13	GENIC	possibly homozygous	51747163
10	94449132	94449133	G	A	23	GENIC	homozygous	51747165
10	94449182	94449183	A	C	26	GENIC	homozygous	51747167
10	94449203	94449204	C	A	24	GENIC	homozygous	51747169
10	94450058	94450059	G	T	18	GENIC	homozygous	51747171
10	94450087	94450088	C	T	17	GENIC	homozygous	51548904
10	94450467	94450468	C	T	39	GENIC	homozygous	51747173
10	94451081	94451082	G	-	1	GENIC	homozygous	51747177
10	94451217	94451218	C	A	35	GENIC	heterozygous	51936848
10	94451220	94451221	G	A	33	GENIC	heterozygous	51936851
10	94451342	94451343	C	T	26	GENIC	heterozygous	51747183
10	94451349	94451350	C	A	27	GENIC	heterozygous	51747185
10	94451352	94451353	G	A	27	GENIC	heterozygous	51747188
10	94451587	94451588	T	G	35	GENIC	homozygous	51747190
10	94451635	94451636	T	C	32	GENIC	homozygous	51548908