chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15695479	15695480	A	-	5	GENIC	homozygous	45097277
X	15697473	15697474	G	A	16	GENIC	homozygous	45097279
X	15697497	15697498	G	A	11	GENIC	possibly homozygous	45097280
X	15699571	15699572	C	T	15	GENIC	homozygous	45097281
X	15699582	15699583	C	G	17	GENIC	possibly homozygous	45097282
X	15699822	15699823	G	T	10	GENIC	possibly homozygous	45473715
X	15700195	15700196	A	C	12	GENIC	homozygous	45473717
X	15700610	15700611	C	G	17	GENIC	possibly homozygous	45473719
X	15701243	15701244	C	-	3	GENIC	homozygous	45473721
X	15701906	15701907	T	C	19	GENIC	homozygous	45097286
X	15703931	15703932	T	C	31	GENIC	possibly homozygous	45097288
X	15708864	15708865	G	A	7	GENIC	homozygous	45097292