chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	20038848	20038849	C	T	11	GENIC	homozygous	108236278
X	20044918	20044919	G	C	6	GENIC	homozygous	125101268
X	20044972	20044973	G	C	7	GENIC	homozygous	108236284
X	20044985	20044986	G	C	8	GENIC	homozygous	125101269
X	20050119	20050120	A	G	4	GENIC	homozygous	125101270
X	20050981	20050982	G	A	5	GENIC	homozygous	125101271
X	20053069	20053070	T	C	10	GENIC	homozygous	108236286
X	20053884	20053885	T	A	4	GENIC	homozygous	108236288
X	20058326	20058327	G	A	11	GENIC	homozygous	108236296
X	20059824	20059825	T	G	4	GENIC	homozygous	119909152
X	20060773	20060774	G	T	9	GENIC	homozygous	108236298
X	20062297	20062298	C	T	8	GENIC	homozygous	108236300
X	20063257	20063258	A	T	6	GENIC	homozygous	108236302
X	20064054	20064055	C	T	10	GENIC	homozygous	108236307
X	20064119	20064120	T	C	16	GENIC	homozygous	108236309
X	20066941	20066942	A	G	11	GENIC	homozygous	108236313
X	20067553	20067554	C	A	10	GENIC	homozygous	108236315
X	20067791	20067792	A	G	11	GENIC	homozygous	108236317
X	20069049	20069050	A	G	11	GENIC	homozygous	108236319