chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71397594	71397596	CC	--	41	GENIC	homozygous	50821817
11	71398455	71398456	T	C	18	GENIC	homozygous	50821818
11	71399510	71399511	C	G	27	GENIC	homozygous	50821820
11	71399951	71399952	A	ATT	35	GENIC	homozygous	50821822
11	71400400	71400401	C	T	31	GENIC	homozygous	50821823
11	71400984	71400985	G	A	5	GENIC	heterozygous	50821825
11	71401136	71401137	A	AT	26	GENIC	heterozygous	50821827
11	71406320	71406321	T	A	25	GENIC	homozygous	50821831
11	71409489	71409490	G	C	18	GENIC	heterozygous	50821833
11	71411724	71411725	C	T	32	GENIC	homozygous	50821836
11	71412310	71412311	C	T	16	GENIC	homozygous	50821838
11	71413150	71413151	A	ACC	6	GENIC	heterozygous	50821840
11	71413150	71413151	A	AC	6	GENIC	heterozygous	50821841
11	71415300	71415301	A	G	31	GENIC	possibly homozygous	50821843
11	71415598	71415599	T	C	36	GENIC	possibly homozygous	50821845
11	71416061	71416062	C	T	32	GENIC	homozygous	50821847
11	71416083	71416084	G	A	32	GENIC	homozygous	50821849
11	71417077	71417078	G	A	36	GENIC	homozygous	50821851
11	71417958	71417959	A	AT	36	GENIC	homozygous	50821852
11	71419101	71419102	T	C	45	GENIC	heterozygous	50961471