chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	13436846	13436848	GT		12	GENIC	possibly homozygous	141061091
X	13448138	13448139	C	T	9	GENIC	heterozygous	403684263
X	13448138	13448139	C		9	GENIC	heterozygous	403684264