chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
MT	13822	13823	C	T	6618	GENIC	possibly homozygous	109049494
MT	13879	13880	C	A	6495	GENIC	possibly homozygous	109024987
MT	13974	13975	G	A	6837	GENIC	possibly homozygous	109024989