chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	117091374	117091375	G	C	30	GENIC	homozygous	140688893
X	117091659	117091659		T	25	GENIC	homozygous	140594037
X	117091716	117091717	G	A	22	GENIC	homozygous	140688894
X	117092922	117092923	G	A	7	GENIC	homozygous	140688895
X	117093887	117093887		AT	17	GENIC	homozygous	140594038
X	117097620	117097621	A	G	1	GENIC	homozygous	145226201
X	117097950	117097951	A	G	15	GENIC	homozygous	140688896
X	117098699	117098700	C	T	18	GENIC	homozygous	140688897
X	117100030	117100031	C	T	25	GENIC	homozygous	140688898
X	117100253	117100254	C	T	19	GENIC	homozygous	140688899
X	117103528	117103529	G	T	22	GENIC	homozygous	140688900
X	117103543	117103544	C	T	24	GENIC	homozygous	140688901
X	117104047	117104048	A	G	27	GENIC	homozygous	140688902
X	117104336	117104337	T	C	18	GENIC	homozygous	140688903
X	117107365	117107366	G	C	23	GENIC	homozygous	140688904
X	117107480	117107481	C	T	25	GENIC	homozygous	140688905
X	117097487	117097488	G	A	5	GENIC	homozygous	403487378
X	117097487	117097488	G		5	GENIC	heterozygous	403487379