chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	153555542	153555543	T	G	11	GENIC	homozygous	108353737
X	153577755	153577756	C	G	14	GENIC	homozygous	108461914
X	153598807	153598808	G	A	17	GENIC	homozygous	108353743
X	153598810	153598811	C	A	16	GENIC	homozygous	108353745
X	153598870	153598871	C	A	19	GENIC	homozygous	108353747
X	153602136	153602137	C	T	8	GENIC	homozygous	108353749
X	153602157	153602158	C	T	11	GENIC	homozygous	108353751
X	153602220	153602221	C	T	10	GENIC	homozygous	108353753
X	153618899	153618900	C	T	13	GENIC	heterozygous	108461915
X	153644852	153644853	T	C	15	GENIC	homozygous	108461917
X	153646402	153646403	T	C	7	GENIC	homozygous	108461919
X	153646535	153646536	G	A	7	GENIC	homozygous	108461921
X	153646544	153646545	G	A	10	GENIC	homozygous	108461923
X	153772165	153772166	G	T	15	GENIC	homozygous	108353767
X	153836513	153836514	T	G	13	GENIC	possibly homozygous	108353772
X	154021206	154021207	G	T	11	GENIC	heterozygous	108461925