chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	70729035	70729036	T	C	19	GENIC	homozygous	108273130
X	70759747	70759748	A	G	11	GENIC	homozygous	108273132
X	70759814	70759815	T	C	16	GENIC	homozygous	108273134
X	70759815	70759816	C	A	16	GENIC	homozygous	108273136
X	70759898	70759899	A	T	19	GENIC	homozygous	108273138
X	70759899	70759900	C	A	19	GENIC	homozygous	108273140
X	70784083	70784084	A	G	11	GENIC	homozygous	108273142
X	70792905	70792906	T	G	14	GENIC	homozygous	108449761
X	70829714	70829715	A	C	16	GENIC	homozygous	108273152
X	70829760	70829761	T	G	18	GENIC	homozygous	108273154
X	70829867	70829868	A	G	21	GENIC	homozygous	108273158
X	70838217	70838218	G	A	16	GENIC	homozygous	108273166
X	70838258	70838259	T	C	21	GENIC	homozygous	108273168
X	70841228	70841229	C	T	9	GENIC	homozygous	108551471