chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15454597	15454598	T	C	39	GENIC	homozygous	108233394
X	15454629	15454630	C	T	34	GENIC	homozygous	108233396
X	15454784	15454785	C	A	30	GENIC	homozygous	108233398
X	15454913	15454914	G	A	39	GENIC	homozygous	108233400
X	15455953	15455954	C	G	32	GENIC	homozygous	108369870
X	15456491	15456499	TTGAGTAG		26	GENIC	homozygous	129722686
X	15457050	15457052	TG		12	GENIC	homozygous	129722687
X	15457284	15457285	T	C	29	GENIC	homozygous	108233402
X	15457294	15457295	C	T	29	GENIC	homozygous	108233404
X	15457698	15457699	C	T	35	GENIC	homozygous	108233406
X	15458010	15458011	T	C	27	GENIC	homozygous	108233408
X	15459032	15459033	C	T	28	GENIC	homozygous	108233410