chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69375919	69375920	C	CATT	22	GENIC	homozygous	51485159
10	69376082	69376084	CA	--	10	GENIC	heterozygous	52383754
10	69383928	69383929	G	-	3	GENIC	homozygous	52383756
10	69383930	69383931	T	TGCTTG	2	GENIC	homozygous	52383758
10	69383935	69383936	G	GCA	1	GENIC	homozygous	52383760
10	69390559	69390560	G	-	6	GENIC	heterozygous	52383764
10	69391088	69391089	C	CA	3	GENIC	homozygous	52383766
10	69397406	69397408	TG	--	4	GENIC	heterozygous	51687133
10	69397948	69397949	G	GTC	1	GENIC	homozygous	52441302
10	69400064	69400065	T	G	39	GENIC	homozygous	51485215
10	69408344	69408345	C	CA	22	GENIC	homozygous	51485230
10	69408354	69408355	G	-	20	GENIC	homozygous	51485231
10	69411336	69411337	G	-	10	GENIC	possibly homozygous	51687143
10	69425096	69425097	T	TC	10	GENIC	homozygous	51485257