chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	62394250	62394251	C	T	12	GENIC	homozygous	108267283
X	62394271	62394272	G	T	13	GENIC	homozygous	108267285
X	62394284	62394285	A	T	13	GENIC	homozygous	108267287
X	62394306	62394307	G	A	10	GENIC	homozygous	108267289
X	62394313	62394314	C	G	8	GENIC	homozygous	108267291
X	62394322	62394323	C	A	8	GENIC	homozygous	108267293
X	62394324	62394325	T	A	8	GENIC	homozygous	108267295
X	62394359	62394360	A	T	13	GENIC	homozygous	108267297
X	62394368	62394369	C	T	13	GENIC	homozygous	108267299
X	62394369	62394370	T	A	11	GENIC	homozygous	108267301
X	62394380	62394381	T	A	11	GENIC	homozygous	108267303
X	62394390	62394391	T	G	12	GENIC	homozygous	108267305
X	62394397	62394398	G	A	12	GENIC	homozygous	108267307
X	62394415	62394416	C	A	14	GENIC	homozygous	108267309
X	62406251	62406252	T	A	5	GENIC	homozygous	108382289
X	62406273	62406274	G	C	8	GENIC	homozygous	108267311
X	62406275	62406276	T	G	8	GENIC	homozygous	108267313
X	62451801	62451802	T	C	14	GENIC	heterozygous	108608465
X	62570643	62570644	G	T	12	GENIC	homozygous	108267461
X	62578776	62578777	T	A	16	GENIC	homozygous	108267485
X	62620241	62620242	T	C	9	GENIC	homozygous	108382291
X	62656576	62656577	A	G	11	GENIC	homozygous	108267710
X	62661812	62661813	G	T	16	GENIC	homozygous	108267712
X	62661852	62661853	G	T	14	GENIC	homozygous	108267714
X	62662764	62662765	A	C	13	GENIC	homozygous	108267716
X	62662765	62662766	C	A	13	GENIC	homozygous	108267718
X	62678285	62678286	T	C	16	GENIC	homozygous	108382293
X	62678335	62678336	A	C	12	GENIC	homozygous	108382295
X	62678336	62678337	C	A	11	GENIC	homozygous	108267732
X	62685371	62685372	C	A	1	GENIC	homozygous	108608467
X	62685737	62685738	A	T	15	GENIC	homozygous	108267748
X	62685819	62685820	C	A	10	GENIC	homozygous	108267750
X	62685887	62685888	A	G	17	GENIC	homozygous	108267752
X	62685888	62685889	G	A	17	GENIC	homozygous	108267754