chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
MT	5326	5327	C	T	248	GENIC	possibly homozygous	109018214
MT	5559	5560	G	A	249	GENIC	possibly homozygous	109024914
MT	5742	5743	A	G	243	GENIC	possibly homozygous	109024917
MT	6009	6010	C	T	250	GENIC	possibly homozygous	109049444
MT	6438	6439	T	C	247	GENIC	possibly homozygous	109024920
MT	6597	6598	C	T	250	GENIC	homozygous	109049447
MT	6663	6664	C	T	250	GENIC	homozygous	109024923
MT	6768	6769	A	G	246	GENIC	possibly homozygous	109049450
MT	6786	6787	C	T	249	GENIC	possibly homozygous	109049453
MT	6825	6826	C	T	250	GENIC	possibly homozygous	109049456