chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	45081265	45081266	C	T	5	GENIC	homozygous	108489743
X	45081308	45081309	T	C	13	GENIC	homozygous	108489745
X	45086646	45086647	G	A	8	GENIC	homozygous	108489747
X	45096499	45096500	C	A	9	GENIC	homozygous	108489749
X	45098929	45098930	C	T	13	GENIC	homozygous	108489751
X	45098987	45098988	A	G	7	GENIC	homozygous	108489753
X	45099397	45099398	C	T	12	GENIC	homozygous	108489755
X	45101562	45101563	G	A	11	GENIC	homozygous	108489757
X	45105699	45105700	G	A	11	GENIC	homozygous	108489759
X	45108529	45108530	T	A	7	GENIC	homozygous	108489761
X	45113773	45113774	T	C	11	GENIC	homozygous	108489767
X	45108540	45108541	C	T	9	GENIC	homozygous	108489763
X	45109408	45109409	G	A	10	GENIC	homozygous	108489765
X	45114427	45114428	A	G	13	GENIC	homozygous	108489769
X	45119066	45119067	A	G	16	GENIC	homozygous	108489771