chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
MT	2836	2837	C	T	3000	GENIC	possibly homozygous	109049418
MT	2928	2929	C	T	2931	GENIC	possibly homozygous	109049421
MT	3000	3001	C	T	3085	GENIC	possibly homozygous	109049424
MT	3429	3430	T	C	3194	GENIC	possibly homozygous	109049427
MT	3435	3436	C	T	3187	GENIC	possibly homozygous	109049430
MT	3483	3484	C	T	3067	GENIC	homozygous	109049433