chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15172514	15172515	A		30	GENIC	homozygous	129722537
X	15172916	15172917	A	G	27	GENIC	homozygous	108233178
X	15174197	15174198	A	G	25	GENIC	homozygous	108233180
X	15174619	15174619		C	23	GENIC	possibly homozygous	129722538
X	15177442	15177442		GTGTGG	30	GENIC	homozygous	129722540
X	15174949	15174950	T	C	11	GENIC	homozygous	129808825
X	15175672	15175673	T	C	16	GENIC	homozygous	125100855
X	15177846	15177847	T	G	41	GENIC	homozygous	108233182
X	15178321	15178322	A	G	27	GENIC	homozygous	108233184
X	15179012	15179013	A	T	31	GENIC	homozygous	108233186
X	15180270	15180271	C	T	22	GENIC	homozygous	108233188
X	15180721	15180722	G	A	27	GENIC	homozygous	108233190
X	15182306	15182306		CC	24	GENIC	homozygous	129722541