chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94446140	94446141	A	AAAAG	42	GENIC	homozygous	51747159
10	94446424	94446425	A	G	21	GENIC	homozygous	51548898
10	94447117	94447118	T	C	35	GENIC	homozygous	51548899
10	94447208	94447209	A	G	31	GENIC	homozygous	51548900
10	94448512	94448513	A	G	29	GENIC	homozygous	51747161
10	94448548	94448549	C	CA	20	GENIC	homozygous	51936842
10	94449132	94449133	G	A	34	GENIC	homozygous	51747165
10	94449182	94449183	A	C	31	GENIC	homozygous	51747167
10	94449203	94449204	C	A	31	GENIC	homozygous	51747169
10	94450058	94450059	G	T	45	GENIC	homozygous	51747171
10	94450087	94450088	C	T	47	GENIC	homozygous	51548904
10	94450467	94450468	C	T	37	GENIC	homozygous	51747173
10	94451002	94451003	G	A	27	GENIC	heterozygous	51936845
10	94451008	94451009	C	T	29	GENIC	heterozygous	51747175
10	94451081	94451082	G	-	3	GENIC	homozygous	51747177
10	94451083	94451084	C	-	3	GENIC	homozygous	51747179
10	94451086	94451087	G	A	13	GENIC	heterozygous	51747181
10	94451217	94451218	C	A	38	GENIC	heterozygous	51936848
10	94451220	94451221	G	A	38	GENIC	heterozygous	51936851
10	94451342	94451343	C	T	36	GENIC	heterozygous	51747183
10	94451349	94451350	C	A	40	GENIC	heterozygous	51747185
10	94451352	94451353	G	A	39	GENIC	possibly homozygous	51747188
10	94451587	94451588	T	G	38	GENIC	homozygous	51747190
10	94451635	94451636	T	C	43	GENIC	homozygous	51548908