chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	85559002	85559003	C	A	27	GENIC	homozygous	50853794
11	85626903	85626904	A	G	14	GENIC	heterozygous	50853865
11	85644616	85644617	T	C	6	GENIC	homozygous	50853866
11	85644663	85644664	A	C	4	GENIC	homozygous	50853867
11	85644674	85644675	G	C	3	GENIC	homozygous	50853868
11	85704427	85704429	GT	--	15	GENIC	homozygous	50853870
11	85704428	85704429	T	TTTTTG	11	GENIC	homozygous	50853871
11	85704798	85704799	T	C	33	GENIC	homozygous	50853872
11	85705274	85705275	G	T	51	GENIC	homozygous	50853873
11	85705361	85705370	ACCTGCTTA	---------	18	GENIC	homozygous	50853874
11	85705367	85705368	T	TC	18	GENIC	heterozygous	50853875
11	85705373	85705374	T	A	26	GENIC	heterozygous	50853876
11	85707457	85707461	ACAT	----	16	GENIC	possibly homozygous	50853877
11	85709644	85709645	G	C	43	GENIC	homozygous	50853878
11	85711286	85711287	A	AT	5	GENIC	homozygous	50853879
11	85711304	85711305	A	-	2	GENIC	homozygous	50853880
11	85711742	85711743	C	CAAA	5	GENIC	homozygous	50853881
11	85567472	85567478	GTGTGT	------	12	GENIC	heterozygous	50973245
11	85567474	85567478	GTGT	----	12	GENIC	heterozygous	50973246
11	85626933	85626934	G	A	19	GENIC	heterozygous	50898212