chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	65960357	65960358	T	C	33	GENIC	homozygous	46190682
19	65960566	65960567	G	GT	35	GENIC	homozygous	46190683
19	65960770	65960771	A	-	20	GENIC	homozygous	46190685
19	65960906	65960907	A	AAATG	9	GENIC	homozygous	46190686
19	65961767	65961768	C	CTT	1	GENIC	homozygous	46474387
19	65962789	65962790	A	G	29	GENIC	homozygous	46190687
19	65964473	65964474	A	T	18	GENIC	homozygous	46190688
19	65964563	65964567	ATAT	----	16	GENIC	homozygous	46190689
19	65964991	65964992	G	T	29	GENIC	homozygous	46190691
19	65965004	65965005	G	T	28	GENIC	homozygous	46190692
19	65966147	65966148	T	C	30	GENIC	possibly homozygous	46190693
19	65966224	65966225	A	G	31	GENIC	homozygous	46190694