chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	7337573	7337573		T	52	GENIC	possibly homozygous	131743626
16	7337582	7337583	C	T	53	GENIC	homozygous	112346367
16	7337740	7337741	T		39	GENIC	homozygous	131171814
16	7337846	7337847	T	A	51	GENIC	homozygous	112346369
16	7338380	7338381	G	A	52	GENIC	homozygous	112346371
16	7338686	7338687	C	T	52	GENIC	homozygous	112346373
16	7338734	7338735	G	A	52	GENIC	homozygous	112346375
16	7339424	7339428	TCTG		47	GENIC	homozygous	131743627
16	7345271	7345272	A	G	55	GENIC	homozygous	131746966
16	7340435	7340436	G	A	57	GENIC	homozygous	112346378
16	7340437	7340438	T	G	57	GENIC	homozygous	112346380
16	7344158	7344159	T	C	56	GENIC	possibly homozygous	112346382