chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	17681279	17681280	T	A	8	GENIC	homozygous	62915985
X	17682563	17682564	C	G	31	GENIC	homozygous	62915986
X	17683351	17683352	G	A	11	GENIC	homozygous	62915987
X	17686892	17686893	A	T	8	GENIC	homozygous	62915988
X	17690694	17690695	T	C	20	GENIC	homozygous	62915989
X	17695479	17695480	A	G	16	GENIC	homozygous	62915990
X	17701458	17701459	A	T	19	GENIC	homozygous	62915991
X	17701835	17701836	A	T	7	GENIC	homozygous	62915992
X	17702707	17702708	A	T	10	GENIC	homozygous	62915993
X	17709886	17709887	T	C	11	GENIC	possibly homozygous	62915995
X	17713708	17713709	G	A	7	GENIC	homozygous	62916000
X	17722941	17722942	C	T	9	GENIC	homozygous	62916001
X	17724663	17724664	C	T	13	GENIC	possibly homozygous	62916002