chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	53926693	53926694	G	A	16	GENIC	homozygous	111247657
17	53927225	53927226	A	G	33	GENIC	homozygous	111530760
17	53931922	53931923	C	T	20	GENIC	homozygous	111530764
17	53934602	53934603	T	G	32	GENIC	homozygous	111402566
17	53934603	53934604	G	A	32	GENIC	homozygous	111530766
17	53934606	53934607	G	A	30	GENIC	homozygous	111530768
17	53934981	53934982	T	C	31	GENIC	homozygous	111530770
17	53935396	53935397	T	C	29	GENIC	homozygous	111530772
17	53938182	53938183	G	T	30	GENIC	homozygous	111247667
17	53940050	53940051	A	G	20	GENIC	homozygous	111247675
17	53940205	53940206	C	A	32	GENIC	homozygous	111247677
17	53941726	53941727	T	C	21	GENIC	homozygous	111247679
17	53944102	53944103	T	G	12	GENIC	homozygous	111530774
17	53945425	53945426	C	T	29	GENIC	homozygous	111530778
17	53942290	53942291	T	C	24	GENIC	homozygous	111063702
17	53949007	53949008	C	A	41	GENIC	homozygous	111530780
17	53952974	53952975	C	A	20	GENIC	homozygous	111063706
17	53953742	53953743	A	G	7	GENIC	heterozygous	111656141
17	53953880	53953881	T	A	18	GENIC	possibly homozygous	111530782