chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71398455	71398456	T	C	21	GENIC	homozygous	50821818
11	71399510	71399511	C	G	25	GENIC	homozygous	50821820
11	71402357	71402358	G	A	20	GENIC	homozygous	50961459
11	71402807	71402808	C	T	24	GENIC	homozygous	50891669
11	71404779	71404780	T	-	16	GENIC	homozygous	50961460
11	71404983	71404984	A	G	19	GENIC	homozygous	50961461
11	71406320	71406321	T	A	26	GENIC	homozygous	50821831
11	71406361	71406362	T	C	27	GENIC	homozygous	50992404
11	71407613	71407614	G	C	31	GENIC	homozygous	50992405
11	71409420	71409421	G	T	29	GENIC	homozygous	50992406
11	71409474	71409475	T	-	29	GENIC	possibly homozygous	50992407
11	71409476	71409477	T	-	18	GENIC	possibly homozygous	50992408
11	71409489	71409490	G	C	14	GENIC	homozygous	50821833
11	71409874	71409875	C	G	25	GENIC	homozygous	50992409
11	71410444	71410448	AAAA	----	2	GENIC	heterozygous	50821835
11	71410447	71410448	A	-	2	GENIC	heterozygous	51284134
11	71411724	71411725	C	T	33	GENIC	homozygous	50821836
11	71413150	71413151	A	ACCC	1	GENIC	homozygous	50961462
11	71414258	71414259	T	C	18	GENIC	homozygous	50961463
11	71414997	71414998	G	GTC	17	GENIC	possibly homozygous	50961464
11	71415288	71415289	C	T	22	GENIC	homozygous	50961465
11	71415300	71415301	A	G	27	GENIC	homozygous	50821843
11	71415598	71415599	T	C	29	GENIC	homozygous	50821845
11	71417959	71417960	T	-	9	GENIC	homozygous	50961467
11	71418214	71418215	C	T	24	GENIC	homozygous	50891693
11	71418729	71418730	T	A	24	GENIC	homozygous	50961468