chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	107757774	107757775	G	C	2	GENIC	homozygous	108597518
X	107757775	107757776	C	T	2	GENIC	homozygous	108597520
X	107757776	107757777	G	T	2	GENIC	homozygous	108597522