chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124832735	124832736	G	T	17	GENIC	homozygous	108326421
X	124837749	124837750	A		5	GENIC	homozygous	129787274
X	124837950	124837950		ATAC	12	GENIC	homozygous	129787275
X	124841051	124841051		TTAAATA	10	GENIC	homozygous	129787276
X	124841670	124841671	A	T	13	GENIC	homozygous	108326427
X	124841779	124841780	C	G	17	GENIC	homozygous	108326429
X	124844265	124844266	T	C	19	GENIC	homozygous	108326431
X	124846567	124846568	A	G	14	GENIC	homozygous	108326433
X	124847011	124847012	G	A	10	GENIC	homozygous	108326435
X	124847428	124847429	C	T	8	GENIC	homozygous	108326437
X	124850004	124850005	A		9	GENIC	homozygous	129787277
X	124853953	124853958	AAAAC		7	GENIC	homozygous	129787278
X	124856399	124856400	A		11	GENIC	homozygous	129787279
X	124856655	124856655		GT	10	GENIC	homozygous	129787280
X	124856726	124856727	C	T	7	GENIC	homozygous	108326439
X	124862366	124862366		A	8	GENIC	homozygous	129787281
X	124865594	124865594		A	13	GENIC	homozygous	129787282
X	124867794	124867794		TGTCCTCTTGAC	10	GENIC	homozygous	129787283
X	124843733	124843734	C	T	9	GENIC	homozygous	108424745
X	124858341	124858342	A	C	10	GENIC	homozygous	108326441
X	124862443	124862444	C	T	13	GENIC	homozygous	108326443
X	124867439	124867440	G	A	10	GENIC	homozygous	108326445