chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	54029312	54029313	T	G	37	GENIC	homozygous	111247743
17	54035636	54035637	G	A	34	GENIC	homozygous	111247745
17	54040103	54040104	A	G	32	GENIC	homozygous	111063824
17	54040413	54040414	T	C	34	GENIC	homozygous	111247747
17	54040883	54040884	A	T	25	GENIC	homozygous	111063826
17	54043945	54043946	C	A	22	GENIC	possibly homozygous	111247749
17	54045929	54045930	T	A	22	GENIC	homozygous	111063834
17	54046741	54046742	C	T	26	GENIC	homozygous	111247751
17	54048956	54048957	G	A	19	GENIC	homozygous	111063837
17	54049201	54049202	T	G	25	GENIC	homozygous	111247753
17	54050412	54050413	A	G	18	GENIC	homozygous	111063839
17	54050815	54050816	C	T	9	GENIC	homozygous	111247755
17	54052103	54052104	C	A	36	GENIC	homozygous	111247757
17	54053235	54053236	C	A	25	GENIC	homozygous	111063842
17	54057394	54057395	C	A	19	GENIC	homozygous	111063849
17	54058979	54058980	A	G	21	GENIC	homozygous	111247759
17	54060296	54060297	G	A	36	GENIC	heterozygous	111063853
17	54062849	54062850	G	A	34	GENIC	homozygous	111205142
17	54067847	54067848	T	C	35	GENIC	homozygous	111063856
17	54069991	54069992	G	A	28	GENIC	homozygous	111247761
17	54070192	54070193	G	T	19	GENIC	homozygous	111063859