chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	53092493	53092494	C	T	26	GENIC	homozygous	47327804
17	53093095	53093096	T	G	27	GENIC	homozygous	47132483
17	53093150	53093151	T	G	5	GENIC	homozygous	47132484
17	53093152	53093153	A	G	6	GENIC	homozygous	47132485
17	53093208	53093209	G	C	14	GENIC	homozygous	47132486
17	53093515	53093517	GT	--	8	GENIC	possibly homozygous	47132487
17	53093629	53093630	T	TA	15	GENIC	homozygous	47132488
17	53093663	53093664	C	T	22	GENIC	possibly homozygous	47132489
17	53093765	53093766	T	C	16	GENIC	possibly homozygous	47132490
17	53093901	53093902	A	G	23	GENIC	possibly homozygous	47132491
17	53094404	53094405	A	T	15	GENIC	possibly homozygous	47132492
17	53094453	53094454	A	G	11	GENIC	homozygous	47132493
17	53094456	53094457	G	A	10	GENIC	homozygous	47132494
17	53099289	53099290	G	C	11	GENIC	possibly homozygous	47327808
17	53099582	53099583	T	A	4	GENIC	heterozygous	47132506
17	53099611	53099614	GGG	---	1	GENIC	homozygous	47132507
17	53099626	53099627	A	G	5	GENIC	homozygous	47709925
17	53101084	53101085	G	A	27	GENIC	homozygous	47327812
17	53101143	53101144	A	C	11	GENIC	homozygous	47327814
17	53101153	53101154	A	C	16	GENIC	homozygous	47327816
17	53101308	53101309	G	A	18	GENIC	homozygous	47132516
17	53101318	53101319	C	T	23	GENIC	homozygous	47327818
17	53101373	53101374	C	G	16	GENIC	homozygous	47327820
17	53101391	53101392	G	A	14	GENIC	homozygous	47327822
17	53102071	53102072	G	T	22	GENIC	possibly homozygous	47327824