chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	32118647	32118648	C	T	28	GENIC	homozygous	108252281
X	32119000	32119001	T	A	14	GENIC	possibly homozygous	108252283
X	32122822	32122823	C	T	32	GENIC	homozygous	108252285
X	32124854	32124855	C	A	30	GENIC	homozygous	108252287
X	32124964	32124965	G	C	31	GENIC	homozygous	108252289
X	32125328	32125329	A	T	13	GENIC	homozygous	108252291
X	32126556	32126557	C	G	17	GENIC	homozygous	108252293
X	32137111	32137112	A	T	23	GENIC	heterozygous	108252295
X	32138363	32138364	C	T	13	GENIC	possibly homozygous	108478783
X	32138501	32138502	C	T	25	GENIC	homozygous	108252299
X	32139728	32139729	C	T	27	GENIC	possibly homozygous	108252301