chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	28261655	28261656	T	C	30	GENIC	homozygous	145979864
X	28261957	28261958	T	C	29	GENIC	homozygous	149464312
X	28264076	28264077	C	G	36	GENIC	homozygous	149464313
X	28265040	28265041	T	C	27	GENIC	homozygous	145979867
X	28265146	28265147	G	A	21	GENIC	homozygous	149464314
X	28265774	28265775	G	A	22	GENIC	homozygous	145979868
X	28266049	28266050	A	T	28	GENIC	homozygous	149464315
X	28266768	28266769	C	T	26	GENIC	homozygous	149464316
X	28266999	28266999		TGTATGTCTAAATTAGACAAATTACCCTC	32	GENIC	homozygous	145969486
X	28267386	28267387	G	T	29	GENIC	homozygous	145979870
X	28267515	28267516	C	T	34	GENIC	homozygous	149464317
X	28264010	28264011	G	A	27	GENIC	homozygous	147231681
X	28268857	28268858	A	G	34	GENIC	homozygous	145979871
X	28269919	28269920	T	C	38	GENIC	homozygous	145979872
X	28270425	28270426	T	A	48	GENIC	homozygous	145979873
X	28272042	28272042		A	31	GENIC	homozygous	145969487
X	28272929	28272930	T	C	30	GENIC	homozygous	149464318
X	28275009	28275010	C	A	26	GENIC	homozygous	147231695
X	28277897	28277898	A	G	22	GENIC	homozygous	149464319
X	28275350	28275351	G		33	GENIC	possibly homozygous	404421997
X	28275350	28275351	G	A	33	GENIC	heterozygous	404421998