chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45295457	45295458	C	A	34	GENIC	homozygous	51442171
10	45295584	45295585	G	A	42	GENIC	homozygous	51442172
10	45296404	45296405	C	CTTTTTT	8	GENIC	homozygous	51442173
10	45296422	45296423	C	T	25	GENIC	heterozygous	51636184
10	45297863	45297864	T	C	41	GENIC	homozygous	51442174
10	45298059	45298060	C	-	26	GENIC	homozygous	51442175
10	45299180	45299184	AAAT	----	6	GENIC	homozygous	51442176
10	45299201	45299202	A	-	8	GENIC	homozygous	51442177
10	45299422	45299426	CTCG	----	14	GENIC	possibly homozygous	51442178
10	45299431	45299432	T	TCG	16	GENIC	heterozygous	51442179
10	45299437	45299438	G	T	21	GENIC	possibly homozygous	51442180
10	45299439	45299440	G	T	21	GENIC	possibly homozygous	51442181
10	45299443	45299444	G	T	22	GENIC	homozygous	51442182
10	45301315	45301316	G	GAA	3	GENIC	heterozygous	51442183
10	45301315	45301316	G	GAAA	3	GENIC	heterozygous	51442184
10	45301716	45301717	A	AAAAAAAG	17	GENIC	homozygous	51442185
10	45301960	45301961	T	TA	8	GENIC	homozygous	51442186
10	45302585	45302586	C	T	36	GENIC	homozygous	51442187
10	45303140	45303141	T	A	19	GENIC	homozygous	51442188
10	45303308	45303309	T	C	22	GENIC	homozygous	51442189
10	45303587	45303588	T	G	30	GENIC	homozygous	51442190
10	45304860	45304861	C	CAAAA	1	GENIC	homozygous	51442191
10	45305035	45305036	A	ATG	11	GENIC	possibly homozygous	51442192
10	45305066	45305067	T	TGC	6	GENIC	heterozygous	51873325
10	45307033	45307034	A	-	11	GENIC	homozygous	51442194