chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	20038848	20038849	C	T	17	GENIC	homozygous	108236278
X	20040432	20040433	C	A	4	GENIC	homozygous	108777610
X	20042598	20042599	T	A	15	GENIC	homozygous	108236280
X	20042599	20042600	C	A	15	GENIC	homozygous	108236282
X	20044972	20044973	G	C	18	GENIC	homozygous	108236284
X	20053069	20053070	T	C	31	GENIC	homozygous	108236286
X	20053884	20053885	T	A	16	GENIC	homozygous	108236288
X	20054099	20054100	C	T	15	GENIC	homozygous	108236290
X	20055771	20055772	A	C	11	GENIC	homozygous	108236292
X	20056678	20056679	A	G	19	GENIC	homozygous	108236294
X	20058326	20058327	G	A	15	GENIC	homozygous	108236296
X	20062297	20062298	C	T	15	GENIC	homozygous	108236300
X	20063257	20063258	A	T	15	GENIC	homozygous	108236302
X	20063717	20063718	G	A	23	GENIC	homozygous	108236304
X	20064054	20064055	C	T	30	GENIC	homozygous	108236307
X	20064119	20064120	T	C	25	GENIC	homozygous	108236309
X	20059703	20059704	C	T	21	GENIC	homozygous	108371873
X	20066941	20066942	A	G	29	GENIC	homozygous	108236313
X	20067553	20067554	C	A	24	GENIC	homozygous	108236315
X	20067791	20067792	A	G	23	GENIC	homozygous	108236317
X	20069049	20069050	A	G	17	GENIC	homozygous	108236319