chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71397594	71397596	CC	--	20	GENIC	homozygous	50821817
11	71398455	71398456	T	C	24	GENIC	homozygous	50821818
11	71399510	71399511	C	G	20	GENIC	homozygous	50821820
11	71400984	71400985	G	A	3	GENIC	heterozygous	50821825
11	71401136	71401137	A	AT	13	GENIC	heterozygous	50821827
11	71402807	71402808	C	T	29	GENIC	homozygous	50891669
11	71406069	71406070	C	G	4	GENIC	homozygous	50891677
11	71406089	71406090	C	G	7	GENIC	homozygous	50891679
11	71406320	71406321	T	A	14	GENIC	homozygous	50821831
11	71409489	71409490	G	C	21	GENIC	heterozygous	50821833
11	71410231	71410232	C	T	13	GENIC	heterozygous	50891681
11	71411724	71411725	C	T	31	GENIC	homozygous	50821836
11	71414258	71414259	T	C	16	GENIC	homozygous	50961463
11	71402357	71402358	G	A	26	GENIC	homozygous	50961459
11	71404779	71404780	T	-	16	GENIC	possibly homozygous	50961460
11	71404983	71404984	A	G	30	GENIC	homozygous	50961461
11	71413150	71413151	A	ACCC	3	GENIC	homozygous	50961462
11	71414997	71414998	G	GTC	10	GENIC	possibly homozygous	50961464
11	71415288	71415289	C	T	24	GENIC	homozygous	50961465
11	71415300	71415301	A	G	25	GENIC	homozygous	50821843
11	71415598	71415599	T	C	18	GENIC	homozygous	50821845
11	71417492	71417493	A	C	24	GENIC	heterozygous	50961466
11	71417959	71417960	T	-	9	GENIC	homozygous	50961467
11	71418214	71418215	C	T	28	GENIC	homozygous	50891693
11	71418729	71418730	T	A	34	GENIC	homozygous	50961468
11	71419060	71419061	A	G	20	GENIC	heterozygous	50961469
11	71419097	71419098	T	C	17	GENIC	heterozygous	50961470
11	71419101	71419102	T	C	17	GENIC	heterozygous	50961471
11	71419105	71419106	T	C	20	GENIC	heterozygous	50891695
11	71419109	71419110	T	C	17	GENIC	possibly homozygous	50891697