chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	66069991	66069992	C	T	7	GENIC	homozygous	45417694
X	66072758	66072759	T	TC	8	GENIC	heterozygous	45145101
X	66085605	66085606	C	T	13	GENIC	heterozygous	45417706
X	66085628	66085629	C	T	9	GENIC	heterozygous	45417708
X	66080589	66080590	A	G	11	GENIC	heterozygous	45872585
X	66086537	66086538	G	A	9	GENIC	heterozygous	45417710
X	66087737	66087738	A	G	11	GENIC	heterozygous	45145164
X	66088603	66088604	A	G	9	GENIC	heterozygous	45417712
X	66089220	66089221	A	G	11	GENIC	heterozygous	45145167
X	66089877	66089878	C	T	10	GENIC	heterozygous	45417715
X	66090592	66090593	G	A	7	GENIC	heterozygous	45145168
X	66091284	66091285	T	G	10	GENIC	heterozygous	45915791
X	66099654	66099655	A	ACT	8	GENIC	heterozygous	45719402
X	66111244	66111245	T	C	8	GENIC	heterozygous	45719418
X	66094618	66094619	G	A	7	GENIC	heterozygous	45379940
X	66095834	66095835	T	C	11	GENIC	heterozygous	45962469
X	66111278	66111279	G	A	8	GENIC	heterozygous	45962471
X	66124718	66124730	TGTGTCTGTGTC	------------	7	GENIC	heterozygous	45915798
X	66125716	66125717	T	C	9	GENIC	heterozygous	45719428
X	66127827	66127828	T	G	10	GENIC	heterozygous	45379954
X	66129039	66129040	G	GT	12	GENIC	heterozygous	45719436
X	66130725	66130726	G	A	11	GENIC	heterozygous	45732555