chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	51066011	51066012	C	T	25	GENIC	homozygous	112506419
15	51066027	51066028	G	A	23	GENIC	homozygous	112506421
15	51067371	51067372	A	G	28	GENIC	homozygous	112506423
15	51067372	51067373	G	A	30	GENIC	possibly homozygous	112506425
15	51067446	51067447	T	C	36	GENIC	homozygous	112506427
15	51067448	51067449	C	T	36	GENIC	homozygous	112506429
15	51067629	51067630	G	C	29	GENIC	homozygous	112506431