chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94195327	94195328	C	A	38	GENIC	homozygous	51746415
10	94195363	94195364	G	A	40	GENIC	homozygous	51746417
10	94196297	94196298	T	C	32	GENIC	homozygous	51548246
10	94197058	94197060	CT	--	22	INTERGENIC	homozygous	51746419
10	94197185	94197186	G	A	38	GENIC	homozygous	51548247
10	94197625	94197626	A	G	31	GENIC	homozygous	51746421
10	94198408	94198409	G	T	38	GENIC	homozygous	51548248
10	94198487	94198488	T	C	34	GENIC	homozygous	51548249
10	94198514	94198515	C	T	35	GENIC	homozygous	51548250
10	94198525	94198526	C	A	32	GENIC	homozygous	51548251
10	94199165	94199166	T	-	14	GENIC	homozygous	51746423
10	94199743	94199744	T	C	39	GENIC	homozygous	51746425
10	94200297	94200298	G	A	24	GENIC	homozygous	51746427
10	94200889	94200890	C	G	41	GENIC	possibly homozygous	51548253
10	94201292	94201293	G	C	38	GENIC	homozygous	51548254
10	94201757	94201758	G	A	32	GENIC	homozygous	51746429
10	94201950	94201951	A	G	27	GENIC	homozygous	51548255
10	94202084	94202085	A	G	41	GENIC	homozygous	51548256
10	94203861	94203862	T	C	38	GENIC	homozygous	51548257
10	94204870	94204871	A	G	57	GENIC	possibly homozygous	51548258