chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	10406180	10406181	G	A	5	GENIC	homozygous	108224346
X	10408380	10408381	G	A	9	GENIC	homozygous	108224348
X	10409964	10409965	T	C	14	GENIC	possibly homozygous	108366761
X	10411703	10411704	A	T	7	GENIC	homozygous	108224352
X	10412823	10412824	G	A	10	GENIC	homozygous	108789611