chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69375919	69375920	C	CATT	8	GENIC	homozygous	51485159
10	69379221	69379222	T	C	9	GENIC	homozygous	52846493
10	69383928	69383929	G	-	2	GENIC	homozygous	52383756
10	69383930	69383931	T	TGCTTG	1	GENIC	homozygous	52383758
10	69383935	69383936	G	GCA	2	GENIC	homozygous	52383760
10	69383938	69383939	T	C	3	GENIC	homozygous	52383762
10	69390558	69390560	GG	--	3	GENIC	heterozygous	51485191
10	69391433	69391434	C	CAGCAG	2	GENIC	homozygous	52846497
10	69407233	69407234	G	GTGCA	5	GENIC	heterozygous	51485228
10	69408344	69408345	C	CA	11	GENIC	homozygous	51485230
10	69408354	69408355	G	-	13	GENIC	homozygous	51485231
10	69411336	69411337	G	-	11	GENIC	homozygous	51687143
10	69416089	69416090	G	-	5	GENIC	heterozygous	51485247
10	69425096	69425097	T	TC	3	GENIC	homozygous	51485257
10	69388329	69388330	C	-	3	GENIC	heterozygous	52320567
10	69396826	69396827	G	A	6	GENIC	homozygous	52159972
10	69396936	69396937	C	T	6	GENIC	homozygous	52159973
10	69397955	69397957	TC	--	3	GENIC	heterozygous	52461201