chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
MT	11798	11799	T	C	860	GENIC	homozygous	140848939
MT	11831	11832	T	C	902	GENIC	homozygous	140848940
MT	11918	11919	T	C	897	GENIC	possibly homozygous	140848941
MT	12035	12036	C	T	955	GENIC	homozygous	140848943
MT	12068	12069	T	C	965	GENIC	possibly homozygous	140848944
MT	12173	12174	A	G	930	GENIC	homozygous	140848945
MT	12350	12351	T	C	745	GENIC	possibly homozygous	140848946
MT	12635	12636	T	C	952	GENIC	homozygous	140848947
MT	12860	12861	G	A	850	GENIC	homozygous	140848948
MT	13001	13002	T	C	738	GENIC	homozygous	140848949
MT	13208	13209	C	T	819	GENIC	homozygous	140848950
MT	13478	13479	G	A	833	GENIC	possibly homozygous	140848951
MT	12494	12495	G	A	862	GENIC	possibly homozygous	146002983