chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15454597	15454598	T	C	17	GENIC	homozygous	108233394
X	15454629	15454630	C	T	13	GENIC	homozygous	108233396
X	15454784	15454785	C	A	19	GENIC	homozygous	108233398
X	15454913	15454914	G	A	29	GENIC	homozygous	108233400
X	15457284	15457285	T	C	15	GENIC	homozygous	108233402
X	15457294	15457295	C	T	16	GENIC	homozygous	108233404
X	15457698	15457699	C	T	32	GENIC	homozygous	108233406
X	15458010	15458011	T	C	8	GENIC	homozygous	108233408
X	15459032	15459033	C	T	23	GENIC	homozygous	108233410