chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	82376149	82376150	C	T	20	GENIC	possibly homozygous	115921876
11	82376700	82376701	C	T	24	GENIC	homozygous	115921878
11	82377167	82377168	T	A	30	GENIC	homozygous	115921880
11	82377464	82377465	T	C	31	GENIC	homozygous	115921882
11	82377813	82377814	A	G	28	GENIC	homozygous	115921884
11	82380204	82380205	T	G	22	GENIC	possibly homozygous	115921886
11	82382491	82382492	A	G	27	GENIC	homozygous	115921888
11	82382725	82382726	T	C	21	GENIC	homozygous	115921890
11	82382796	82382797	C	T	33	GENIC	homozygous	115921892
11	82383280	82383281	G	A	23	GENIC	homozygous	115921894
11	82383828	82383829	C	T	29	GENIC	homozygous	115921896
11	82384826	82384827	A	T	30	GENIC	homozygous	115921898
11	82384827	82384828	T	C	30	GENIC	homozygous	115921900
11	82385513	82385514	A	G	18	GENIC	homozygous	115921902
11	82386285	82386286	C	T	24	GENIC	homozygous	115921904
11	82387076	82387077	T	C	26	GENIC	homozygous	115921906
11	82387105	82387106	G	T	31	GENIC	homozygous	115921908
11	82387244	82387245	A	G	33	GENIC	homozygous	115921910
11	82388139	82388140	A	G	12	GENIC	homozygous	115921912
11	82388165	82388166	G	A	12	GENIC	homozygous	116068333
11	82390692	82390693	T	A	37	GENIC	homozygous	115921914