chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	158967106	158967107	T	C	59	GENIC	homozygous	119965738
X	158969665	158969666	A	G	85	GENIC	possibly homozygous	108354629
X	158970700	158970701	C	T	61	GENIC	homozygous	108354631
X	158971594	158971595	T	C	56	GENIC	possibly homozygous	108354633
X	158971692	158971693	G	A	77	GENIC	homozygous	108354635
X	158974621	158974622	G	C	50	GENIC	homozygous	108354637
X	158975579	158975580	A	G	61	GENIC	homozygous	108354639
X	158977754	158977755	T	C	65	GENIC	homozygous	108354641
X	158978349	158978350	A	T	64	GENIC	homozygous	108354643
X	158978387	158978388	G	A	57	GENIC	homozygous	108354645