chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	50421267	50421269	GT	--	7	GENIC	heterozygous	51183861
11	50427954	50427955	C	A	16	GENIC	homozygous	50955721
11	50427956	50427957	T	A	16	GENIC	homozygous	50955723
11	50427520	50427521	T	TCAAA	10	GENIC	possibly homozygous	50774868
11	50427928	50427929	G	A	14	GENIC	homozygous	50774870
11	50427950	50427951	G	A	16	GENIC	homozygous	50774871
11	50427965	50427967	TG	--	19	GENIC	homozygous	51183865
11	50427972	50427973	T	A	20	GENIC	homozygous	50774873
11	50427974	50427975	G	A	21	GENIC	homozygous	50774874
11	50427976	50427977	G	A	21	GENIC	homozygous	50774875
11	50427978	50427979	A	ACACACAC	21	GENIC	homozygous	51183867
11	50427981	50427982	C	CCA	19	GENIC	homozygous	51183869
11	50427983	50427985	TT	--	19	GENIC	homozygous	51183871
11	50440236	50440237	C	-	27	GENIC	homozygous	50774882
11	50440244	50440245	C	CT	26	GENIC	homozygous	50774883
11	50440385	50440386	G	A	22	GENIC	homozygous	50774884
11	50440389	50440390	G	-	22	GENIC	homozygous	50774885
11	50440932	50440933	C	-	3	GENIC	heterozygous	50774886
11	50444650	50444651	A	G	11	GENIC	homozygous	50774888
11	50444794	50444795	C	A	15	GENIC	homozygous	50774889
11	50444795	50444796	C	A	15	GENIC	homozygous	50774890