chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	64258707	64258708	T	C	21	GENIC	homozygous	145104746
X	64258798	64258798		A	23	GENIC	homozygous	142744796
X	64259000	64259001	C	T	18	GENIC	homozygous	142758581
X	64259506	64259507	C	G	22	GENIC	homozygous	142758582
X	64259675	64259676	T	C	28	GENIC	homozygous	142758583
X	64259898	64259899	A	G	20	GENIC	homozygous	142758584
X	64260048	64260049	T	C	19	GENIC	homozygous	142758585
X	64260177	64260178	C		25	GENIC	homozygous	142744797
X	64260906	64260907	C	G	28	GENIC	homozygous	142758586
X	64262989	64262990	G	A	25	GENIC	homozygous	142758587
X	64263319	64263320	C	A	21	GENIC	homozygous	142758588
X	64264821	64264822	A	C	24	GENIC	homozygous	142758589
X	64265596	64265597	G	A	20	GENIC	homozygous	142758590
X	64268448	64268449	G	A	27	GENIC	homozygous	142758591
X	64269569	64269570	C	T	33	GENIC	homozygous	142758592