chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15938207	15938208	T	C	11	GENIC	homozygous	45097830
X	15939137	15939138	T	C	10	GENIC	homozygous	45097831
X	15940181	15940182	A	-	12	GENIC	homozygous	45097832
X	15940285	15940287	AC	--	10	GENIC	homozygous	45097833
X	15940480	15940481	G	T	12	GENIC	possibly homozygous	45097834
X	15941046	15941047	T	C	5	GENIC	homozygous	45097835
X	15941323	15941324	T	TTAAAAAGTAGATGGGGGCTGGAGAGATGGCTCAGCCGTTAAAGGCTAGGCTCACAACCAAAAATA	11	GENIC	homozygous	45501287
X	15942121	15942122	G	A	4	GENIC	homozygous	45097836
X	15942414	15942415	A	AAAAGAAAGAAAG	1	GENIC	homozygous	45628927
X	15942703	15942704	C	-	2	GENIC	homozygous	45097837
X	15942713	15942714	G	-	2	GENIC	homozygous	45097838
X	15942725	15942726	C	G	1	GENIC	homozygous	45252136
X	15942764	15942765	G	T	3	GENIC	heterozygous	45097839
X	15942850	15942851	T	C	3	GENIC	homozygous	45097842
X	15944405	15944406	T	TG	3	GENIC	heterozygous	45501289
X	15944408	15944409	G	GGGGCTCGAGACCCCAAAAGTACAAC	4	GENIC	heterozygous	45501291
X	15944791	15944792	T	C	13	GENIC	homozygous	45097844
X	15944801	15944802	G	A	10	GENIC	homozygous	45097845
X	15944857	15944859	AA	--	4	GENIC	heterozygous	45501293
X	15944858	15944859	A	-	4	GENIC	heterozygous	45501295
X	15944950	15944951	C	T	15	GENIC	homozygous	45097847
X	15945284	15945285	G	-	11	GENIC	homozygous	45097848
X	15946520	15946521	C	T	19	GENIC	homozygous	45097849