chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	62394250	62394251	C	T	7	GENIC	homozygous	108267283
X	62394271	62394272	G	T	5	GENIC	homozygous	108267285
X	62394306	62394307	G	A	5	GENIC	homozygous	108267289
X	62394359	62394360	A	T	6	GENIC	homozygous	108267297
X	62428705	62428706	C	G	3	GENIC	heterozygous	125131086
X	62472337	62472338	G	A	5	GENIC	heterozygous	125131087
X	62600729	62600730	A	T	4	GENIC	heterozygous	125131088
X	62614292	62614293	G	A	4	GENIC	heterozygous	125131089
X	62470085	62470086	C	G	6	GENIC	heterozygous	125105636
X	62476242	62476243	G	A	5	GENIC	heterozygous	125105637
X	62618391	62618392	C	A	7	GENIC	heterozygous	125105639
X	62635210	62635211	G	A	12	GENIC	homozygous	125105642
X	62650510	62650511	C	G	3	GENIC	heterozygous	125131090
X	62650523	62650524	G	C	3	GENIC	heterozygous	125131091
X	62650772	62650773	G	A	7	GENIC	heterozygous	125105643
X	62656576	62656577	A	G	6	GENIC	homozygous	108267710
X	62662005	62662006	G	A	4	GENIC	heterozygous	125131092
X	62678285	62678286	T	C	8	GENIC	homozygous	108382293
X	62688848	62688849	A	G	8	GENIC	heterozygous	120053191