chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	14633648	14633649	G	A	27	GENIC	possibly homozygous	108232390
X	14635532	14635533	C	T	22	GENIC	homozygous	108232392
X	14635605	14635606	T	C	26	GENIC	homozygous	108232394
X	14635951	14635952	G	A	30	GENIC	homozygous	108232396
X	14635978	14635979	C	A	27	GENIC	homozygous	108232398
X	14636970	14636971	T	G	17	GENIC	homozygous	108232400
X	14637452	14637453	C	A	13	GENIC	homozygous	119905179
X	14637582	14637583	A	C	23	GENIC	homozygous	108369718
X	14637885	14637886	G	T	18	GENIC	homozygous	108232402
X	14638539	14638540	G	T	22	GENIC	possibly homozygous	108232404
X	14640457	14640458	G	A	16	GENIC	possibly homozygous	108232406
X	14642030	14642031	A	T	19	GENIC	homozygous	108232408