chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15699571	15699572	C	T	14	GENIC	homozygous	45097281
X	15699582	15699583	C	G	15	GENIC	homozygous	45097282
X	15700610	15700611	C	G	6	GENIC	heterozygous	45473719
X	15701243	15701244	C	-	12	GENIC	homozygous	45473721
X	15701906	15701907	T	C	10	GENIC	homozygous	45097286
X	15702094	15702098	TTTT	----	13	GENIC	possibly homozygous	45807367
X	15700899	15700900	G	A	7	GENIC	homozygous	45807364
X	15700972	15700973	T	G	9	GENIC	homozygous	45807365
X	15701153	15701154	G	T	7	GENIC	homozygous	45807366
X	15703680	15703681	G	A	9	GENIC	possibly homozygous	45807368
X	15703931	15703932	T	C	11	GENIC	homozygous	45097288
X	15704253	15704254	C	T	13	GENIC	homozygous	45807369
X	15704795	15704796	T	G	10	GENIC	homozygous	45273864
X	15704798	15704799	T	C	10	GENIC	possibly homozygous	45807370
X	15706007	15706008	G	A	16	GENIC	homozygous	45097289
X	15706051	15706054	TTC	---	12	GENIC	heterozygous	45501151
X	15703313	15703314	G	GTT	3	GENIC	homozygous	45585108