chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	32118647	32118648	C	T	39	GENIC	homozygous	108252281
X	32119000	32119001	T	A	73	GENIC	possibly homozygous	108252283
X	32122822	32122823	C	T	69	GENIC	homozygous	108252285
X	32124854	32124855	C	A	54	GENIC	homozygous	108252287
X	32124964	32124965	G	C	58	GENIC	possibly homozygous	108252289
X	32125328	32125329	A	T	80	GENIC	homozygous	108252291
X	32126556	32126557	C	G	78	GENIC	homozygous	108252293
X	32134291	32134292	G	T	203	GENIC	heterozygous	119992873
X	32134301	32134302	T	G	188	GENIC	heterozygous	119992875
X	32134346	32134347	C	T	240	GENIC	heterozygous	119992877
X	32134367	32134368	G	A	221	GENIC	heterozygous	119992879
X	32134377	32134378	T	G	239	GENIC	heterozygous	119992881
X	32134383	32134384	C	G	245	GENIC	heterozygous	119992883
X	32135700	32135701	A	C	144	GENIC	heterozygous	119992885
X	32137111	32137112	A	T	82	GENIC	heterozygous	108252295
X	32138501	32138502	C	T	55	GENIC	homozygous	108252299
X	32139728	32139729	C	T	59	GENIC	possibly homozygous	108252301
X	32141688	32141689	G	A	20	GENIC	heterozygous	119992887
X	32135822	32135823	G	C	120	GENIC	heterozygous	119913836
X	32136861	32136862	C	A	87	GENIC	heterozygous	119913838
X	32136864	32136865	C	T	89	GENIC	heterozygous	119913840
X	32136949	32136950	A	T	96	GENIC	heterozygous	119913842
X	32144521	32144522	A	G	46	GENIC	homozygous	119913844
X	32138363	32138364	C	T	38	GENIC	homozygous	108478783