chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	52117041	52117042	A	G	41	GENIC	homozygous	112062732
16	52117354	52117355	T	G	28	GENIC	homozygous	112062734
16	52117799	52117800	T	G	25	GENIC	homozygous	112062735
16	52118382	52118383	T	C	35	GENIC	homozygous	112062736
16	52120256	52120257	G	A	34	GENIC	homozygous	112062737
16	52121466	52121467	C	A	41	GENIC	homozygous	112062738
16	52122661	52122662	C	T	52	GENIC	homozygous	112062739
16	52123713	52123714	G	T	36	GENIC	homozygous	112309053
16	52123840	52123841	T	C	44	GENIC	homozygous	112062740
16	52123992	52123993	C	T	34	GENIC	homozygous	112062741
16	52124141	52124142	A	G	45	GENIC	homozygous	112062742
16	52124556	52124557	C	A	51	GENIC	possibly homozygous	112062743
16	52125620	52125621	G	A	42	GENIC	homozygous	112062744
16	52125846	52125847	T	C	53	GENIC	homozygous	112062745