chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15938207	15938208	T	C	26	GENIC	homozygous	45097830
X	15939137	15939138	T	C	40	GENIC	homozygous	45097831
X	15940181	15940182	A	-	24	GENIC	possibly homozygous	45097832
X	15940285	15940287	AC	--	24	GENIC	homozygous	45097833
X	15940480	15940481	G	T	27	GENIC	homozygous	45097834
X	15941046	15941047	T	C	28	GENIC	homozygous	45097835
X	15942121	15942122	G	A	31	GENIC	homozygous	45097836
X	15942703	15942704	C	-	3	GENIC	homozygous	45097837
X	15942713	15942714	G	-	1	GENIC	homozygous	45097838
X	15942764	15942765	G	T	1	GENIC	homozygous	45097839
X	15942790	15942791	T	G	4	GENIC	homozygous	45097840
X	15942800	15942801	T	C	4	GENIC	homozygous	45097841
X	15942850	15942851	T	C	6	GENIC	homozygous	45097842
X	15944403	15944404	G	C	13	GENIC	heterozygous	45097843
X	15944791	15944792	T	C	18	GENIC	homozygous	45097844
X	15944801	15944802	G	A	17	GENIC	homozygous	45097845
X	15944857	15944858	A	-	2	GENIC	homozygous	45097846
X	15944950	15944951	C	T	18	GENIC	homozygous	45097847
X	15945284	15945285	G	-	21	GENIC	homozygous	45097848
X	15946520	15946521	C	T	28	GENIC	homozygous	45097849