chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124832735	124832736	G	T	13	GENIC	homozygous	108326421
X	124841670	124841671	A	T	18	GENIC	homozygous	108326427
X	124841779	124841780	C	G	11	GENIC	homozygous	108326429
X	124843733	124843734	C	T	10	GENIC	homozygous	108424745
X	124844265	124844266	T	C	9	GENIC	homozygous	108326431
X	124846567	124846568	A	G	19	GENIC	homozygous	108326433
X	124847011	124847012	G	A	17	GENIC	homozygous	108326435
X	124847428	124847429	C	T	23	GENIC	homozygous	108326437
X	124856726	124856727	C	T	28	GENIC	homozygous	108326439
X	124858341	124858342	A	C	14	GENIC	homozygous	108326441
X	124862443	124862444	C	T	23	GENIC	homozygous	108326443
X	124867439	124867440	G	A	17	GENIC	homozygous	108326445