chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	63342987	63342988	C	T	26	GENIC	homozygous	108268972
X	63344628	63344629	C	T	5	GENIC	homozygous	108268974
X	63350156	63350157	C	A	12	GENIC	homozygous	108268977
X	63351473	63351474	A	G	14	GENIC	homozygous	108268979
X	63353029	63353030	T	C	17	GENIC	homozygous	108268981
X	63353189	63353190	T	A	10	GENIC	homozygous	108268983
X	63353944	63353945	C	G	6	GENIC	homozygous	108268985
X	63354153	63354154	T	C	15	GENIC	homozygous	108268987
X	63355701	63355702	G	T	6	GENIC	homozygous	108268989
X	63353782	63353783	G	C	17	GENIC	homozygous	108501417
X	63363780	63363781	A	G	24	GENIC	homozygous	108268991
X	63364181	63364182	T	G	7	GENIC	homozygous	108268993
X	63366693	63366694	A	T	3	GENIC	homozygous	108268995
X	63371571	63371572	A	T	4	GENIC	homozygous	108268997
X	63371658	63371659	G	A	10	GENIC	homozygous	108268999
X	63377965	63377966	C	G	12	GENIC	homozygous	108269001
X	63382653	63382654	T	G	7	GENIC	homozygous	108382720
X	63385092	63385093	C	T	12	GENIC	homozygous	108269005