chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	46991579	46991580	G	C	9	GENIC	heterozygous	125125523
X	46995349	46995350	C	T	8	GENIC	homozygous	108794726
X	46995424	46995425	G	T	7	GENIC	heterozygous	108819903
X	47008316	47008317	T	C	8	GENIC	homozygous	108732010
X	47009839	47009840	A	G	11	GENIC	homozygous	108492331
X	47012714	47012715	T	C	7	GENIC	homozygous	108707763
X	47014062	47014063	A	G	8	GENIC	homozygous	108707765
X	47014395	47014396	T	G	8	GENIC	homozygous	108707767
X	47018770	47018771	G	A	10	GENIC	homozygous	108707771
X	47020297	47020298	T	C	6	GENIC	homozygous	108492343
X	47021260	47021261	T	C	7	GENIC	homozygous	108707775
X	47021922	47021923	C	T	11	GENIC	homozygous	108707777
X	47022045	47022046	G	A	15	GENIC	homozygous	108673382
X	47022954	47022955	G	A	12	GENIC	homozygous	108707779
X	47023445	47023446	G	C	7	GENIC	homozygous	108707781
X	47023944	47023945	G	A	7	GENIC	homozygous	108707783
X	47025892	47025893	T	C	5	GENIC	homozygous	108492347