chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	52017371	52017372	C	T	71	GENIC	homozygous	112062614
16	52017611	52017612	G	A	56	GENIC	possibly homozygous	112062615
16	52017653	52017654	G	A	67	GENIC	homozygous	112062616
16	52017699	52017700	T	A	87	GENIC	possibly homozygous	112062617
16	52017711	52017712	G	T	66	GENIC	homozygous	112062618
16	52018107	52018108	A	G	62	GENIC	homozygous	112062619
16	52018271	52018272	A	G	70	GENIC	homozygous	112062620
16	52018480	52018481	A	G	81	GENIC	homozygous	112062621
16	52018486	52018487	A	G	85	GENIC	homozygous	112062622
16	52019041	52019042	A	T	72	GENIC	homozygous	112062623
16	52019474	52019475	G	C	57	GENIC	homozygous	112062624
16	52019696	52019697	A	G	36	GENIC	homozygous	112435570
16	52019705	52019706	G	A	35	GENIC	possibly homozygous	112435571
16	52019725	52019726	T	C	30	GENIC	possibly homozygous	119166018
16	52020015	52020016	G	A	47	GENIC	homozygous	112062625
16	52020090	52020091	A	G	51	GENIC	homozygous	112062626
16	52020464	52020465	G	A	66	GENIC	homozygous	112062627
16	52020743	52020744	G	A	78	GENIC	homozygous	112062628
16	52021007	52021008	G	A	57	GENIC	possibly homozygous	112062629
16	52021848	52021849	A	T	50	GENIC	homozygous	112062630
16	52023716	52023717	A	C	28	GENIC	homozygous	112062635
16	52022190	52022191	C	T	68	GENIC	homozygous	112062631
16	52022266	52022267	T	C	63	GENIC	homozygous	112062632
16	52023425	52023426	A	C	67	GENIC	homozygous	112062634
16	52025670	52025671	C	T	65	GENIC	heterozygous	119166020
16	52025693	52025694	G	C	81	GENIC	heterozygous	119166022