chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	135093124	135093125	A	G	13	GENIC	homozygous	108509728
X	135095276	135095277	T	C	22	GENIC	homozygous	108509730
X	135095751	135095752	G	T	14	GENIC	homozygous	108509732
X	135097478	135097479	A	C	8	GENIC	homozygous	108509734
X	135097842	135097843	G	A	18	GENIC	homozygous	108509736
X	135099118	135099119	A	G	19	GENIC	homozygous	108509738
X	135099200	135099201	T	C	11	GENIC	homozygous	108509740
X	135099391	135099392	G	A	10	GENIC	homozygous	108509742
X	135100420	135100421	A	G	19	GENIC	homozygous	108509744
X	135100677	135100678	A	G	11	GENIC	homozygous	108509746
X	135103328	135103329	A	G	12	GENIC	homozygous	108509748
X	135103368	135103369	C	T	14	GENIC	homozygous	108509750
X	135103464	135103465	G	A	14	GENIC	homozygous	108509752
X	135107008	135107009	G	A	7	GENIC	homozygous	108509754
X	135107050	135107051	A	T	11	GENIC	homozygous	108509756
X	135107725	135107726	A	G	12	GENIC	homozygous	108509758
X	135108855	135108856	T	G	13	GENIC	homozygous	108509760
X	135109986	135109987	A	G	16	GENIC	homozygous	108509762
X	135111305	135111306	C	T	14	GENIC	homozygous	108509764
X	135111473	135111474	G	A	9	GENIC	homozygous	108509766
X	135112557	135112558	T	G	14	GENIC	homozygous	108509768
X	135113499	135113500	A	G	12	GENIC	homozygous	108509770
X	135113866	135113867	C	T	10	GENIC	homozygous	108509772
X	135114143	135114144	A	G	14	GENIC	homozygous	108509774
X	135116222	135116223	A	C	8	GENIC	homozygous	108509776