chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	61629663	61629664	C	T	60	GENIC	homozygous	140156960
17	61629838	61629839	G	T	53	GENIC	homozygous	140156961
17	61629860	61629861	C	A	56	GENIC	homozygous	140156962
17	61630089	61630093	ACAC		59	GENIC	homozygous	140031524
17	61630095	61630105	GGAAAGAAAC		59	GENIC	homozygous	140031525
17	61630276	61630277	T	A	46	GENIC	homozygous	140156963
17	61630723	61630724	T	C	49	GENIC	homozygous	140156964
17	61630933	61630933		A	47	GENIC	homozygous	140031526
17	61631124	61631130	ATATAC		27	GENIC	homozygous	140031527
17	61631936	61631936		GTACCTGGTGCCCTG	51	GENIC	homozygous	140031528
17	61632542	61632542		GCC	44	GENIC	homozygous	140031529
17	61632544	61632544		A	42	GENIC	homozygous	140031530
17	61632670	61632671	C	A	32	GENIC	heterozygous	403668577
17	61631119	61631120	T	C	31	GENIC	homozygous	155032053
17	61631119	61631120	T		31	GENIC	heterozygous	403668575
17	61632670	61632671	C		32	GENIC	heterozygous	403668576
17	61632670	61632671	C	G	32	GENIC	heterozygous	403668578
17	61632678	61632679	C		30	GENIC	heterozygous	403668579
17	61632678	61632679	C	G	30	GENIC	heterozygous	403668580
17	61632746	61632755	TAGCCTGTC		38	GENIC	homozygous	140031531
17	61632758	61632759	C	G	37	GENIC	homozygous	140156965
17	61633133	61633133		A	40	GENIC	possibly homozygous	140031532
17	61633686	61633687	G	A	52	GENIC	homozygous	140156966
17	61634898	61634899	G		11	GENIC	heterozygous	403418857
17	61634898	61634899	G	C	11	GENIC	heterozygous	403418858
17	61635096	61635097	A	G	30	GENIC	homozygous	140156967
17	61635155	61635155		T	15	GENIC	possibly homozygous	140031533
17	61635411	61635412	C	T	33	GENIC	homozygous	140156968
17	61635414	61635415	T	C	33	GENIC	homozygous	140156969
17	61635831	61635832	A	G	27	GENIC	homozygous	140156970
17	61636998	61636999	G	C	58	GENIC	homozygous	140156971
17	61637005	61637006	A	G	58	GENIC	homozygous	140156972