chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71397594	71397596	CC	--	33	GENIC	homozygous	50821817
11	71398455	71398456	T	C	41	GENIC	homozygous	50821818
11	71399510	71399511	C	G	50	GENIC	possibly homozygous	50821820
11	71399951	71399952	A	ATT	37	GENIC	homozygous	50821822
11	71400400	71400401	C	T	53	GENIC	homozygous	50821823
11	71400984	71400985	G	A	4	GENIC	heterozygous	50821825
11	71401136	71401137	A	AT	17	GENIC	homozygous	50821827
11	71406320	71406321	T	A	36	GENIC	homozygous	50821831
11	71409474	71409475	T	-	36	GENIC	heterozygous	50992407
11	71406175	71406176	T	A	17	GENIC	homozygous	50992403
11	71406361	71406362	T	C	37	GENIC	homozygous	50992404
11	71407613	71407614	G	C	43	GENIC	homozygous	50992405
11	71409420	71409421	G	T	30	GENIC	possibly homozygous	50992406
11	71407926	71407927	A	T	13	GENIC	homozygous	51047480
11	71409476	71409477	T	-	33	GENIC	heterozygous	50992408
11	71409489	71409490	G	C	43	GENIC	heterozygous	50821833
11	71409874	71409875	C	G	40	GENIC	homozygous	50992409
11	71410444	71410448	AAAA	----	3	GENIC	homozygous	50821835
11	71411724	71411725	C	T	44	GENIC	homozygous	50821836
11	71412310	71412311	C	T	17	GENIC	homozygous	50821838
11	71413150	71413151	A	ACC	10	GENIC	heterozygous	50821840
11	71413150	71413151	A	AC	10	GENIC	heterozygous	50821841
11	71415300	71415301	A	G	48	GENIC	homozygous	50821843
11	71415598	71415599	T	C	31	GENIC	possibly homozygous	50821845
11	71416061	71416062	C	T	58	GENIC	homozygous	50821847
11	71416083	71416084	G	A	61	GENIC	possibly homozygous	50821849
11	71417077	71417078	G	A	56	GENIC	homozygous	50821851
11	71417492	71417493	A	C	46	GENIC	heterozygous	50961466
11	71417958	71417959	A	AT	26	GENIC	homozygous	50821852
11	71419105	71419106	T	C	48	GENIC	heterozygous	50891695