chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15743826	15743827	A	C	13	GENIC	possibly homozygous	108370043
X	15744150	15744151	T	G	9	GENIC	homozygous	108370045
X	15744370	15744371	G	T	13	GENIC	homozygous	108370047
X	15744405	15744406	T	C	13	GENIC	homozygous	108370049
X	15746973	15746974	G	A	6	GENIC	homozygous	108233550
X	15748044	15748045	A	T	11	GENIC	homozygous	108370051
X	15752393	15752394	T	C	13	GENIC	homozygous	108370053