chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
MT	11798	11799	T	C	1689	GENIC	possibly homozygous	140848939
MT	11831	11832	T	C	1745	GENIC	possibly homozygous	140848940
MT	11918	11919	T	C	1643	GENIC	possibly homozygous	140848941
MT	12035	12036	C	T	1696	GENIC	homozygous	140848943
MT	12068	12069	T	C	1784	GENIC	possibly homozygous	140848944
MT	12173	12174	A	G	1761	GENIC	homozygous	140848945
MT	12350	12351	T	C	1478	GENIC	possibly homozygous	140848946
MT	12635	12636	T	C	1671	GENIC	possibly homozygous	140848947
MT	12860	12861	G	A	1713	GENIC	homozygous	140848948
MT	13001	13002	T	C	1415	GENIC	possibly homozygous	140848949
MT	13208	13209	C	T	1754	GENIC	homozygous	140848950
MT	13478	13479	G	A	1532	GENIC	possibly homozygous	140848951