chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	53093095	53093096	T	G	14	GENIC	homozygous	47132483
17	53093150	53093151	T	G	7	GENIC	homozygous	47132484
17	53093152	53093153	A	G	7	GENIC	homozygous	47132485
17	53093208	53093209	G	C	16	GENIC	homozygous	47132486
17	53093515	53093517	GT	--	4	GENIC	heterozygous	47132487
17	53093629	53093630	T	TA	13	GENIC	homozygous	47132488
17	53093663	53093664	C	T	18	GENIC	possibly homozygous	47132489
17	53093765	53093766	T	C	17	GENIC	possibly homozygous	47132490
17	53093901	53093902	A	G	10	GENIC	heterozygous	47132491
17	53094404	53094405	A	T	9	GENIC	possibly homozygous	47132492
17	53094453	53094454	A	G	5	GENIC	homozygous	47132493
17	53094456	53094457	G	A	6	GENIC	heterozygous	47132494
17	53095314	53095315	A	G	8	GENIC	possibly homozygous	47132496
17	53095355	53095356	A	G	12	GENIC	homozygous	47132497
17	53095395	53095396	A	AT	2	GENIC	homozygous	47132498
17	53095823	53095824	T	C	6	GENIC	homozygous	47132499
17	53095829	53095830	A	-	1	GENIC	homozygous	47132500
17	53095910	53095911	G	A	11	GENIC	possibly homozygous	47132501
17	53096657	53096658	T	C	8	GENIC	homozygous	47132502
17	53096728	53096729	C	T	9	GENIC	homozygous	47132503
17	53097055	53097056	G	A	8	GENIC	possibly homozygous	47132504
17	53097220	53097221	C	G	11	GENIC	homozygous	47132505
17	53099582	53099583	T	A	8	GENIC	possibly homozygous	47132506
17	53099611	53099614	GGG	---	1	GENIC	homozygous	47132507
17	53099626	53099627	A	G	2	GENIC	homozygous	47709925
17	53099915	53099916	G	A	11	GENIC	homozygous	47132508
17	53100017	53100018	G	A	10	GENIC	heterozygous	47132509
17	53100248	53100249	T	G	12	GENIC	homozygous	47132510
17	53100373	53100374	G	A	9	GENIC	possibly homozygous	47132511
17	53101308	53101309	G	A	12	GENIC	heterozygous	47132516
17	53102021	53102022	G	A	17	GENIC	homozygous	47132517