chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14664061	14664062	T	C	22	GENIC	homozygous	51811403
10	14665828	14665829	G	A	25	GENIC	possibly homozygous	51811405
10	14666494	14666495	G	A	23	GENIC	possibly homozygous	51811407
10	14666538	14666539	C	T	22	GENIC	homozygous	51811409
10	14666652	14666653	C	T	20	GENIC	homozygous	51811411
10	14666857	14666858	A	G	24	GENIC	homozygous	51623467
10	14667477	14667478	T	C	29	GENIC	homozygous	51811413
10	14667649	14667650	T	G	28	GENIC	possibly homozygous	51811415
10	14667937	14667938	G	C	33	GENIC	homozygous	51811417
10	14668562	14668563	A	T	19	GENIC	homozygous	51811419
10	14669004	14669005	C	T	25	GENIC	homozygous	51623469
10	14669535	14669536	G	C	29	GENIC	homozygous	51623470
10	14669608	14669609	T	G	25	GENIC	homozygous	51623471
10	14669665	14669666	C	CAGT	35	GENIC	homozygous	51623472
10	14669700	14669701	C	T	31	GENIC	homozygous	51623473