chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20415186	20415187	G	A	47	GENIC	homozygous	111948632
16	20416321	20416322	G	A	76	GENIC	homozygous	111948634
16	20418953	20418954	T	C	61	GENIC	possibly homozygous	111948636
16	20420138	20420139	A	G	73	GENIC	homozygous	112052882
16	20417631	20417632	G		44	GENIC	homozygous	131173833
16	20418059	20418062	CCA		23	GENIC	heterozygous	131744800
16	20418362	20418363	G	A	62	GENIC	possibly homozygous	112107999
16	20419191	20419192	G	T	48	GENIC	homozygous	112108001
16	20419731	20419732	T	C	53	GENIC	homozygous	112108003
16	20421046	20421047	C	T	63	GENIC	homozygous	111948638
16	20421210	20421211	A	G	51	GENIC	homozygous	111948640
16	20421450	20421451	A	G	60	GENIC	homozygous	111948642
16	20421586	20421587	T		60	GENIC	homozygous	131744801
16	20421708	20421709	G	T	59	GENIC	homozygous	111948644
16	20421978	20421981	GCA		52	GENIC	homozygous	131744802
16	20422691	20422692	G	A	53	GENIC	homozygous	111948646
16	20420629	20420630	T	C	61	GENIC	homozygous	111752792