chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	67242450	67242451	T	G	16	GENIC	homozygous	50807788
11	67244782	67244783	G	GT	22	GENIC	homozygous	50807789
11	67244996	67244999	AAT	---	9	GENIC	homozygous	50807790
11	67245204	67245212	TCTCTCTC	--------	6	GENIC	homozygous	50807792
11	67245370	67245371	C	T	17	GENIC	homozygous	50883232
11	67245371	67245372	C	CTCACACTT	16	GENIC	homozygous	50807793
11	67245394	67245395	C	T	23	GENIC	homozygous	50807795
11	67245440	67245441	C	A	22	GENIC	homozygous	50807797
11	67245708	67245714	AAAAAG	------	6	GENIC	homozygous	50807800
11	67245889	67245890	A	T	11	GENIC	homozygous	50807802
11	67246557	67246558	T	C	15	GENIC	homozygous	50807803
11	67246883	67246884	T	TGG	8	GENIC	homozygous	50807807
11	67246885	67246886	T	G	19	GENIC	possibly homozygous	50807808
11	67246885	67246886	T	TG	10	GENIC	heterozygous	50807810
11	67246885	67246886	T	TGG	10	GENIC	possibly homozygous	50807812
11	67247014	67247015	A	G	23	GENIC	homozygous	50807813
11	67247020	67247021	C	T	24	GENIC	homozygous	50807815
11	67247033	67247034	T	C	24	GENIC	homozygous	50807816
11	67247123	67247124	T	C	21	GENIC	homozygous	50807818
11	67247222	67247223	A	-	19	GENIC	homozygous	50807819
11	67247232	67247233	C	G	21	GENIC	homozygous	50807821
11	67247349	67247350	T	G	14	GENIC	homozygous	50807822
11	67247689	67247691	GT	--	16	GENIC	homozygous	50807823