chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94446140	94446141	A	AAAAG	27	GENIC	homozygous	51747159
10	94446424	94446425	A	G	27	GENIC	homozygous	51548898
10	94447117	94447118	T	C	38	GENIC	homozygous	51548899
10	94447208	94447209	A	G	41	GENIC	homozygous	51548900
10	94448512	94448513	A	G	28	GENIC	possibly homozygous	51747161
10	94448538	94448539	A	AC	22	GENIC	possibly homozygous	51747163
10	94448548	94448549	C	CA	19	GENIC	heterozygous	51936842
10	94449132	94449133	G	A	37	GENIC	homozygous	51747165
10	94449182	94449183	A	C	34	GENIC	homozygous	51747167
10	94449203	94449204	C	A	35	GENIC	homozygous	51747169
10	94450058	94450059	G	T	60	GENIC	homozygous	51747171
10	94450087	94450088	C	T	51	GENIC	homozygous	51548904
10	94450467	94450468	C	T	45	GENIC	homozygous	51747173
10	94451002	94451003	G	A	49	GENIC	heterozygous	51936845
10	94451008	94451009	C	T	47	GENIC	heterozygous	51747175
10	94451051	94451052	A	G	39	GENIC	heterozygous	52167516
10	94451081	94451082	G	-	4	GENIC	heterozygous	51747177
10	94451083	94451084	C	-	2	GENIC	heterozygous	51747179
10	94451086	94451087	G	A	18	GENIC	heterozygous	51747181
10	94451349	94451350	C	A	43	GENIC	possibly homozygous	51747185
10	94451352	94451353	G	A	44	GENIC	possibly homozygous	51747188
10	94451587	94451588	T	G	34	GENIC	homozygous	51747190
10	94451635	94451636	T	C	37	GENIC	homozygous	51548908