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	15942703	15942704	C	-	8	GENIC	homozygous	45097837
X	15942713	15942714	G	-	8	GENIC	homozygous	45097838
X	15942764	15942765	G	T	10	GENIC	homozygous	45097839
X	15942850	15942851	T	C	10	GENIC	homozygous	45097842
X	15943431	15943432	C	T	13	GENIC	homozygous	45274090
X	15944797	15944798	A	G	6	GENIC	homozygous	45274091
X	15944801	15944802	G	A	7	GENIC	homozygous	45097845
X	15944950	15944951	C	T	13	GENIC	homozygous	45097847
X	15942725	15942726	C	G	7	GENIC	homozygous	45252136