chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	44960942	44960943	T	A	13	GENIC	possibly homozygous	108706687
X	44962912	44962913	C	T	13	GENIC	homozygous	108706689
X	44967807	44967808	T	C	13	GENIC	heterozygous	108489577
X	44969422	44969423	T	C	14	GENIC	homozygous	108489579
X	44971691	44971692	A	C	13	GENIC	homozygous	108706691
X	44974820	44974821	C	T	12	GENIC	possibly homozygous	108489585
X	44977685	44977686	C	A	15	GENIC	possibly homozygous	108706693
X	44979363	44979364	A	G	12	GENIC	homozygous	108489591
X	44979739	44979740	C	T	13	GENIC	possibly homozygous	108489593
X	44981796	44981797	A	C	10	GENIC	homozygous	108489597
X	44982178	44982179	A	G	18	GENIC	possibly homozygous	108706695
X	44983416	44983417	A	T	16	GENIC	homozygous	108706697
X	44986394	44986395	C	A	21	GENIC	possibly homozygous	108489601