chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	153555542	153555543	T	G	6	GENIC	homozygous	108353737
X	153598592	153598593	T	A	19	GENIC	homozygous	108735100
X	153598611	153598612	T	G	16	GENIC	homozygous	108530806
X	153598612	153598613	C	A	16	GENIC	homozygous	108530808
X	153598807	153598808	G	A	2	GENIC	homozygous	108353743
X	153598810	153598811	C	A	2	GENIC	homozygous	108353745
X	153598870	153598871	C	A	3	GENIC	homozygous	108353747
X	153602136	153602137	C	T	6	GENIC	homozygous	108353749
X	153602157	153602158	C	T	5	GENIC	homozygous	108353751
X	153602220	153602221	C	T	6	GENIC	homozygous	108353753
X	153646325	153646326	A	C	3	GENIC	homozygous	108735102
X	153646326	153646327	T	A	3	GENIC	homozygous	108735104
X	153730942	153730943	T	A	16	GENIC	heterozygous	108353759
X	153730959	153730960	G	C	16	GENIC	heterozygous	108353761
X	153730961	153730962	A	G	17	GENIC	heterozygous	108353763
X	153731007	153731008	T	A	15	GENIC	heterozygous	108353765
X	153772165	153772166	G	T	13	GENIC	homozygous	108353767
X	153836513	153836514	T	G	5	GENIC	homozygous	108353772
X	153692285	153692286	G	C	7	GENIC	possibly homozygous	108429350