chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	71469734	71469735	C	CGT	9	GENIC	possibly homozygous	45146794
X	71476948	71476949	G	GTC	6	GENIC	heterozygous	45146795
X	71490504	71490505	T	C	11	GENIC	heterozygous	45146796
X	71512308	71512309	G	T	26	GENIC	heterozygous	45146797
X	71519150	71519151	A	AG	23	GENIC	homozygous	45146798