chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15610340	15610341	C	T	11	GENIC	homozygous	108369908
X	15611423	15611424	C	T	18	GENIC	homozygous	108542501
X	15612228	15612229	G	A	9	GENIC	possibly homozygous	108542503