chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	46978965	46978966	G	T	15	GENIC	homozygous	108257570
X	46978977	46978978	G	A	18	GENIC	homozygous	108257572
X	46978978	46978979	A	G	18	GENIC	homozygous	108257574
X	46985317	46985318	A	C	9	GENIC	homozygous	108707755
X	47008767	47008768	A	T	10	GENIC	homozygous	108707757
X	47009839	47009840	A	G	14	GENIC	homozygous	108492331
X	47004609	47004610	T	C	12	GENIC	homozygous	108794728
X	47004354	47004355	C	T	10	GENIC	homozygous	108492325
X	47011337	47011338	C	A	13	GENIC	possibly homozygous	108673380
X	47011466	47011467	A	G	12	GENIC	homozygous	108492333
X	47011554	47011555	C	G	18	GENIC	homozygous	108707759
X	47011814	47011815	C	T	19	GENIC	homozygous	108492335
X	47011850	47011851	A	T	16	GENIC	homozygous	108707761
X	47012714	47012715	T	C	13	GENIC	homozygous	108707763
X	47014062	47014063	A	G	17	GENIC	homozygous	108707765
X	47014395	47014396	T	G	10	GENIC	homozygous	108707767
X	47014985	47014986	G	C	13	GENIC	homozygous	108707769
X	47016608	47016609	A	G	7	GENIC	homozygous	108492341
X	47016754	47016755	T	A	9	GENIC	homozygous	108257576
X	47018770	47018771	G	A	11	GENIC	homozygous	108707771
X	47020897	47020898	A	T	10	GENIC	homozygous	108707773
X	47021260	47021261	T	C	13	GENIC	homozygous	108707775
X	47021922	47021923	C	T	7	GENIC	homozygous	108707777
X	47022045	47022046	G	A	21	GENIC	homozygous	108673382
X	47022954	47022955	G	A	12	GENIC	homozygous	108707779
X	47023445	47023446	G	C	11	GENIC	homozygous	108707781
X	47023944	47023945	G	A	11	GENIC	homozygous	108707783
X	47025892	47025893	T	C	12	GENIC	homozygous	108492347