chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15695462	15695463	G	GAA	15	GENIC	homozygous	45097276
X	15695479	15695480	A	-	14	GENIC	homozygous	45097277
X	15695659	15695660	C	T	29	GENIC	homozygous	45097278
X	15697473	15697474	G	A	29	GENIC	homozygous	45097279
X	15697497	15697498	G	A	25	GENIC	possibly homozygous	45097280
X	15699571	15699572	C	T	18	GENIC	homozygous	45097281
X	15699582	15699583	C	G	20	GENIC	homozygous	45097282
X	15700996	15700997	T	C	19	GENIC	homozygous	45097283
X	15701633	15701634	C	T	31	GENIC	homozygous	45097284
X	15701653	15701654	C	T	32	GENIC	homozygous	45097285
X	15701906	15701907	T	C	17	GENIC	homozygous	45097286
X	15703931	15703932	T	C	17	GENIC	possibly homozygous	45097288
X	15706007	15706008	G	A	13	GENIC	homozygous	45097289
X	15708864	15708865	G	A	13	GENIC	homozygous	45097292
X	15702097	15702098	T	-	11	GENIC	heterozygous	45501147
X	15703313	15703314	G	GTTTT	6	GENIC	heterozygous	45501149
X	15706051	15706054	TTC	---	11	GENIC	heterozygous	45501151
X	15703313	15703314	G	GTT	6	GENIC	heterozygous	45585108
X	15703313	15703314	G	GTTTTT	6	GENIC	heterozygous	45585110
X	15703314	15703315	T	-	6	GENIC	heterozygous	45750633