chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71398455	71398456	T	C	30	GENIC	homozygous	50821818
11	71399510	71399511	C	G	31	GENIC	homozygous	50821820
11	71399951	71399952	A	ATT	24	GENIC	homozygous	50821822
11	71400400	71400401	C	T	33	GENIC	homozygous	50821823
11	71400972	71400973	A	AGAGGAGGAGGAAGAGGAG	7	GENIC	possibly homozygous	51188277
11	71401136	71401137	A	AT	11	GENIC	possibly homozygous	50821827
11	71406051	71406059	TTCTTTCT	--------	4	GENIC	homozygous	51218388
11	71406320	71406321	T	A	37	GENIC	homozygous	50821831
11	71406361	71406362	T	C	25	GENIC	homozygous	50992404
11	71407613	71407614	G	C	31	GENIC	homozygous	50992405
11	71407727	71407728	T	TTG	4	GENIC	heterozygous	51196810
11	71409420	71409421	G	T	26	GENIC	homozygous	50992406
11	71409474	71409475	T	-	24	GENIC	homozygous	50992407
11	71409476	71409477	T	-	14	GENIC	possibly homozygous	50992408
11	71409489	71409490	G	C	20	GENIC	homozygous	50821833
11	71409874	71409875	C	G	25	GENIC	homozygous	50992409
11	71410444	71410448	AAAA	----	10	GENIC	possibly homozygous	50821835
11	71411724	71411725	C	T	27	GENIC	homozygous	50821836
11	71412310	71412311	C	T	23	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	homozygous	50821843
11	71415598	71415599	T	C	29	GENIC	homozygous	50821845
11	71416061	71416062	C	T	29	GENIC	homozygous	50821847
11	71416083	71416084	G	A	33	GENIC	homozygous	50821849
11	71416466	71416467	G	GCACA	9	GENIC	possibly homozygous	51188279
11	71417077	71417078	G	A	42	GENIC	homozygous	50821851
11	71417958	71417959	A	AT	18	GENIC	homozygous	50821852
11	71419050	71419062	AGATAGATAGAT	------------	11	GENIC	homozygous	51188280