chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	65960357	65960358	T	C	44	GENIC	possibly homozygous	46190682
19	65960566	65960567	G	GT	36	GENIC	homozygous	46190683
19	65960769	65960771	AA	--	18	GENIC	homozygous	46190684
19	65960906	65960907	A	AAATG	39	GENIC	homozygous	46190686
19	65961713	65961714	G	A	28	GENIC	homozygous	46353180
19	65961767	65961768	C	CT	8	GENIC	homozygous	46268362
19	65962789	65962790	A	G	41	GENIC	homozygous	46190687
19	65964473	65964474	A	T	33	GENIC	homozygous	46190688
19	65964563	65964567	ATAT	----	24	GENIC	homozygous	46190689
19	65964599	65964600	C	CAGAT	15	GENIC	homozygous	46353182
19	65964991	65964992	G	T	49	GENIC	homozygous	46190691
19	65965004	65965005	G	T	53	GENIC	possibly homozygous	46190692
19	65966147	65966148	T	C	55	GENIC	homozygous	46190693
19	65966224	65966225	A	G	43	GENIC	possibly homozygous	46190694