chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
MT	11798	11799	T	C	1140	GENIC	possibly homozygous	140848939
MT	11831	11832	T	C	1302	GENIC	possibly homozygous	140848940
MT	11918	11919	T	C	1302	GENIC	homozygous	140848941
MT	12035	12036	C	T	1370	GENIC	possibly homozygous	140848943
MT	12068	12069	T	C	1390	GENIC	possibly homozygous	140848944
MT	12173	12174	A	G	1294	GENIC	homozygous	140848945
MT	12350	12351	T	C	1041	GENIC	homozygous	140848946
MT	12494	12495	G	A	1216	GENIC	possibly homozygous	146002983
MT	12635	12636	T	C	1277	GENIC	homozygous	140848947
MT	12860	12861	G	A	1174	GENIC	homozygous	140848948
MT	13001	13002	T	C	1139	GENIC	possibly homozygous	140848949
MT	13208	13209	C	T	1334	GENIC	homozygous	140848950
MT	13478	13479	G	A	1131	GENIC	homozygous	140848951