chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	31126847	31126848	C	T	10	GENIC	homozygous	108250038
X	31127377	31127378	T	C	12	GENIC	homozygous	108250040
X	31127485	31127486	A	G	7	GENIC	homozygous	108250042
X	31128681	31128682	T	G	11	GENIC	homozygous	108478574
X	31129206	31129207	T	C	7	GENIC	homozygous	108250044
X	31129328	31129329	C	T	12	GENIC	possibly homozygous	108250046
X	31130104	31130105	G	T	17	GENIC	homozygous	108250048
X	31130173	31130174	T	A	17	GENIC	homozygous	108250050
X	31130509	31130510	C	T	11	GENIC	homozygous	108250052
X	31132405	31132406	G	A	9	GENIC	homozygous	108250056
X	31133095	31133096	T	C	11	GENIC	homozygous	108250058
X	31134313	31134314	A	T	11	GENIC	homozygous	108250060
X	31135326	31135327	T	C	11	GENIC	homozygous	108250062
X	31135502	31135503	T	G	14	GENIC	homozygous	108250064
X	31135546	31135547	C	T	10	GENIC	homozygous	108250066
X	31135745	31135746	G	A	14	GENIC	homozygous	108250068
X	31136190	31136191	C	T	3	GENIC	homozygous	119913265
X	31137446	31137447	G	A	7	GENIC	homozygous	108250070
X	31137862	31137863	T	C	12	GENIC	homozygous	108250072
X	31138779	31138780	A	G	19	GENIC	possibly homozygous	108250074
X	31139355	31139356	T	A	11	GENIC	homozygous	119913267
X	31139360	31139361	C	G	11	GENIC	homozygous	119913269
X	31139435	31139436	G	A	14	GENIC	homozygous	108478576