chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15699571	15699572	C	T	28	GENIC	homozygous	45097281
X	15699582	15699583	C	G	28	GENIC	homozygous	45097282
X	15700996	15700997	T	C	22	GENIC	homozygous	45097283
X	15701633	15701634	C	T	32	GENIC	homozygous	45097284
X	15701653	15701654	C	T	30	GENIC	homozygous	45097285
X	15701906	15701907	T	C	25	GENIC	homozygous	45097286
X	15702097	15702098	T	-	13	GENIC	heterozygous	45501147
X	15703313	15703314	G	GTTTT	3	GENIC	heterozygous	45501149
X	15703313	15703314	G	GTT	3	GENIC	heterozygous	45585108
X	15703313	15703314	G	GTTTTT	3	GENIC	heterozygous	45585110
X	15703931	15703932	T	C	17	GENIC	homozygous	45097288
X	15706007	15706008	G	A	19	GENIC	homozygous	45097289