chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	50790631	50790632	C	A	21	GENIC	homozygous	116416948
11	50790723	50790724	T	A	22	GENIC	homozygous	115864133
11	50804387	50804388	T	G	37	GENIC	homozygous	115864135
11	50804408	50804409	A	G	39	GENIC	homozygous	115864137
11	50817000	50817001	T	A	3	GENIC	homozygous	118159782
11	50817949	50817950	C	G	9	GENIC	homozygous	118159783
11	50830208	50830209	C	G	13	GENIC	homozygous	118159784
11	50830301	50830302	A	T	13	GENIC	homozygous	116043120
11	50835023	50835024	C	G	39	GENIC	homozygous	116416965
11	50835150	50835151	C	A	48	GENIC	homozygous	115864139
11	50835260	50835261	A	C	29	GENIC	homozygous	115864141
11	50835345	50835346	C	T	3	GENIC	homozygous	116307521
11	50837128	50837129	T	C	15	GENIC	homozygous	116244062
11	50884119	50884120	T	A	22	GENIC	homozygous	115864143
11	50924209	50924210	C	G	62	GENIC	heterozygous	118159785
11	50924229	50924230	T	C	57	GENIC	heterozygous	118159786
11	50924265	50924266	G	T	51	GENIC	heterozygous	118159787
11	50924277	50924278	A	G	44	GENIC	heterozygous	118159788
11	50947486	50947487	A	G	27	GENIC	heterozygous	118159789