chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	18961495	18961496	T	C	24	GENIC	homozygous	112275068
16	18962129	18962130	G		25	GENIC	homozygous	131173613
16	18962537	18962537		GCTGG	29	GENIC	homozygous	131173614
16	18974815	18974815		T	39	GENIC	possibly homozygous	131173616
16	18965454	18965455	G	A	37	GENIC	homozygous	111945713
16	18965562	18965563	A	G	32	GENIC	possibly homozygous	111945716
16	18967773	18967774	A	G	36	GENIC	homozygous	111945718
16	18969508	18969509	T	G	49	GENIC	homozygous	111945720
16	18972558	18972559	A	G	33	GENIC	homozygous	111945722
16	18973550	18973551	T	A	39	GENIC	possibly homozygous	111945724
16	18974819	18974820	T	C	36	GENIC	possibly homozygous	111945726
16	18968013	18968014	G		14	GENIC	homozygous	129339752
16	18970309	18970310	A	G	16	GENIC	homozygous	119192578
16	18972968	18972969	A	G	47	GENIC	homozygous	111750530