chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124832735	124832736	G	T	14	GENIC	homozygous	108326421
X	124833115	124833116	G	A	4	GENIC	homozygous	131249580
X	124834913	124834913		A	6	GENIC	homozygous	131243835
X	124835598	124835599	A	G	8	GENIC	homozygous	131249581
X	124837961	124837962	C	T	6	GENIC	homozygous	131249582
X	124837749	124837750	A		9	GENIC	possibly homozygous	129787274
X	124841670	124841671	A	T	3	GENIC	homozygous	108326427
X	124844265	124844266	T	C	8	GENIC	homozygous	108326431
X	124846567	124846568	A	G	11	GENIC	homozygous	108326433
X	124856399	124856400	A		7	GENIC	homozygous	129787279
X	124856660	124856660		CTCTCACACGTGCTTG	1	GENIC	homozygous	131243836
X	124866077	124866089	TGTCTGTCTGTC		4	GENIC	homozygous	131243837
X	124867439	124867440	G	A	19	GENIC	homozygous	108326445
X	124847428	124847429	C	T	6	GENIC	homozygous	108326437
X	124850885	124850886	T	G	13	GENIC	homozygous	131249583
X	124856726	124856727	C	T	3	GENIC	homozygous	108326439
X	124858341	124858342	A	C	6	GENIC	heterozygous	108326441
X	124862443	124862444	C	T	7	GENIC	homozygous	108326443
X	124866433	124866434	C	T	6	GENIC	homozygous	131249584
X	124843733	124843734	C	T	12	GENIC	homozygous	108424745
X	124867794	124867794		TGTCCTCTTGAC	7	GENIC	homozygous	129787283