chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	135093124	135093125	A	G	23	GENIC	possibly homozygous	108509728
X	135094676	135094676		A	38	GENIC	possibly homozygous	132781819
X	135095276	135095277	T	C	29	GENIC	homozygous	108509730
X	135095428	135095435	TTTCTTT		20	GENIC	homozygous	132781820
X	135095751	135095752	G	T	30	GENIC	homozygous	108509732
X	135096545	135096546	T		36	GENIC	homozygous	132781821
X	135097478	135097479	A	C	37	GENIC	homozygous	108509734
X	135097842	135097843	G	A	33	GENIC	homozygous	108509736
X	135099118	135099119	A	G	47	GENIC	homozygous	108509738
X	135099200	135099201	T	C	30	GENIC	homozygous	108509740
X	135099391	135099392	G	A	31	GENIC	homozygous	108509742
X	135100420	135100421	A	G	34	GENIC	homozygous	108509744
X	135100633	135100634	G		38	GENIC	homozygous	132781822
X	135100677	135100678	A	G	33	GENIC	homozygous	108509746
X	135103328	135103329	A	G	30	GENIC	homozygous	108509748
X	135103368	135103369	C	T	29	GENIC	homozygous	108509750
X	135103464	135103465	G	A	26	GENIC	homozygous	108509752
X	135107008	135107009	G	A	39	GENIC	homozygous	108509754
X	135107050	135107051	A	T	34	GENIC	homozygous	108509756
X	135107725	135107726	A	G	24	GENIC	homozygous	108509758
X	135108855	135108856	T	G	38	GENIC	possibly homozygous	108509760
X	135109986	135109987	A	G	27	GENIC	homozygous	108509762
X	135111305	135111306	C	T	30	GENIC	homozygous	108509764
X	135111473	135111474	G	A	25	GENIC	homozygous	108509766
X	135112557	135112558	T	G	33	GENIC	homozygous	108509768
X	135113499	135113500	A	G	28	GENIC	homozygous	108509770
X	135113866	135113867	C	T	37	GENIC	homozygous	108509772
X	135114143	135114144	A	G	22	GENIC	homozygous	108509774
X	135116175	135116191	TAGCACTCTGATAGAG		50	GENIC	homozygous	132781823
X	135116222	135116223	A	C	45	GENIC	homozygous	108509776
X	135114099	135114100	T	C	29	GENIC	homozygous	108818843
X	135107191	135107192	C	T	19	GENIC	homozygous	120035016
X	135107739	135107740	A	T	22	GENIC	homozygous	108815539