chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	117091374	117091375	G	C	13	GENIC	homozygous	140688893
X	117091659	117091659		T	11	GENIC	homozygous	140594037
X	117091716	117091717	G	A	11	GENIC	homozygous	140688894
X	117092922	117092923	G	A	6	GENIC	homozygous	140688895
X	117093887	117093887		AT	18	GENIC	homozygous	140594038
X	117097950	117097951	A	G	17	GENIC	homozygous	140688896
X	117098699	117098700	C	T	21	GENIC	homozygous	140688897
X	117100030	117100031	C	T	18	GENIC	homozygous	140688898
X	117100253	117100254	C	T	22	GENIC	homozygous	140688899
X	117103528	117103529	G	T	21	GENIC	homozygous	140688900
X	117103543	117103544	C	T	22	GENIC	homozygous	140688901
X	117104047	117104048	A	G	23	GENIC	homozygous	140688902
X	117104336	117104337	T	C	22	GENIC	homozygous	140688903
X	117107365	117107366	G	C	24	GENIC	homozygous	140688904
X	117107480	117107481	C	T	18	GENIC	homozygous	140688905