chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	63342987	63342988	C	T	13	GENIC	homozygous	108268972
X	63344628	63344629	C	T	12	GENIC	homozygous	108268974
X	63349953	63349954	C	A	6	GENIC	heterozygous	108683679
X	63350156	63350157	C	A	6	GENIC	homozygous	108268977
X	63351473	63351474	A	G	8	GENIC	homozygous	108268979
X	63353029	63353030	T	C	10	GENIC	homozygous	108268981
X	63353189	63353190	T	A	3	GENIC	homozygous	108268983
X	63353782	63353783	G	C	6	GENIC	homozygous	108501417
X	63353944	63353945	C	G	10	GENIC	homozygous	108268985
X	63354153	63354154	T	C	6	GENIC	homozygous	108268987
X	63355701	63355702	G	T	14	GENIC	homozygous	108268989
X	63363780	63363781	A	G	9	GENIC	homozygous	108268991
X	63366693	63366694	A	T	7	GENIC	homozygous	108268995
X	63371571	63371572	A	T	7	GENIC	homozygous	108268997
X	63371658	63371659	G	A	6	GENIC	homozygous	108268999
X	63382895	63382896	A	G	8	GENIC	heterozygous	108683680
X	63383852	63383853	T	G	10	GENIC	homozygous	108269003
X	63382896	63382897	T	A	9	GENIC	heterozygous	108683681
X	63383365	63383366	G	T	8	GENIC	homozygous	108683682
X	63383375	63383376	G	T	8	GENIC	homozygous	108683683
X	63383522	63383523	T	C	9	GENIC	homozygous	108683684
X	63383544	63383545	A	G	15	GENIC	homozygous	108551405