chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	110266498	110266499	A	T	46	GENIC	possibly homozygous	45358778
X	110267283	110267284	A	ATC	7	GENIC	homozygous	45193470
X	110267285	110267286	C	A	37	GENIC	heterozygous	45358779
X	110267655	110267656	A	G	49	GENIC	homozygous	45358780
X	110268344	110268345	T	C	49	GENIC	homozygous	45358781
X	110268503	110268504	T	G	38	GENIC	homozygous	45358782
X	110270521	110270522	A	C	34	GENIC	possibly homozygous	45358783