chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15939137	15939138	T	C	7	GENIC	homozygous	45097831
X	15942121	15942122	G	A	10	GENIC	homozygous	45097836
X	15942135	15942136	G	A	13	GENIC	homozygous	45274087
X	15942301	15942302	A	AT	6	GENIC	homozygous	45274088
X	15942313	15942314	A	G	7	GENIC	homozygous	45274089
X	15942703	15942704	C	-	7	GENIC	homozygous	45097837
X	15942713	15942714	G	-	6	GENIC	homozygous	45097838
X	15942725	15942726	C	G	6	GENIC	homozygous	45252136
X	15942764	15942765	G	T	11	GENIC	possibly homozygous	45097839
X	15942790	15942791	T	G	10	GENIC	homozygous	45097840
X	15942800	15942801	T	C	11	GENIC	homozygous	45097841
X	15942850	15942851	T	C	10	GENIC	homozygous	45097842
X	15943431	15943432	C	T	13	GENIC	homozygous	45274090
X	15944797	15944798	A	G	9	GENIC	heterozygous	45274091
X	15944801	15944802	G	A	10	GENIC	heterozygous	45097845
X	15944950	15944951	C	T	13	GENIC	homozygous	45097847
X	15945962	15945968	TTAAAG	------	3	GENIC	heterozygous	45274092
X	15945976	15945977	G	T	5	GENIC	heterozygous	45274093