chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	135190306	135190307	A	G	11	GENIC	homozygous	108509864
X	135190713	135190714	T	G	17	GENIC	homozygous	108509866
X	135190723	135190724	C	T	16	GENIC	homozygous	108509868
X	135191019	135191020	C	A	18	GENIC	homozygous	108509870
X	135191914	135191915	T	A	9	GENIC	homozygous	108509872
X	135192275	135192276	A	G	5	GENIC	homozygous	108509874
X	135192970	135192971	C	T	16	GENIC	homozygous	108509876
X	135193156	135193157	A	G	20	GENIC	homozygous	108509878
X	135193792	135193793	G	C	8	GENIC	homozygous	108509880
X	135195299	135195300	C	T	14	GENIC	homozygous	108509882
X	135199297	135199298	A	G	24	GENIC	homozygous	108509884
X	135199312	135199313	G	A	22	GENIC	homozygous	108509886
X	135199685	135199686	A	G	21	GENIC	homozygous	108509888
X	135201601	135201602	C	T	21	GENIC	homozygous	108509890
X	135204159	135204160	G	A	11	GENIC	homozygous	108509892
X	135204633	135204634	C	T	5	GENIC	homozygous	108509894
X	135205946	135205947	C	T	19	GENIC	homozygous	108509896
X	135208406	135208407	T	C	7	GENIC	homozygous	108509898
X	135209483	135209484	G	A	14	GENIC	homozygous	108509900
X	135212392	135212393	C	T	23	GENIC	homozygous	108509902
X	135213396	135213397	G	A	18	GENIC	homozygous	108509904
X	135217066	135217067	C	A	17	GENIC	homozygous	108509906
X	135222587	135222588	G	C	10	GENIC	possibly homozygous	108509908
X	135223255	135223256	A	G	18	GENIC	homozygous	108509910
X	135223774	135223775	G	T	17	GENIC	homozygous	108509912
X	135223941	135223942	G	A	11	GENIC	homozygous	108509914
X	135224926	135224927	A	C	10	GENIC	homozygous	108509916
X	135225839	135225840	C	T	7	GENIC	homozygous	108509918
X	135227657	135227658	G	A	5	GENIC	homozygous	108509920
X	135230020	135230021	G	A	20	GENIC	homozygous	108509924
X	135231495	135231496	A	T	7	GENIC	homozygous	108509928
X	135232013	135232014	T	C	9	GENIC	homozygous	108509930