chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	21720801	21720802	C	T	82	GENIC	homozygous	108238326
X	21721053	21721054	G	C	76	GENIC	homozygous	108238328
X	21721350	21721351	C	G	64	GENIC	homozygous	108238330
X	21726200	21726201	T	C	41	GENIC	heterozygous	108700983
X	21726208	21726209	C	T	33	GENIC	heterozygous	119909801
X	21732055	21732056	G	C	75	GENIC	heterozygous	119989560
X	21731995	21731996	A	G	77	GENIC	heterozygous	119989552
X	21731997	21731998	C	T	76	GENIC	heterozygous	119989554
X	21732000	21732001	C	T	77	GENIC	heterozygous	119989556
X	21732005	21732006	T	C	82	GENIC	heterozygous	119989558
X	21732061	21732062	C	T	70	GENIC	heterozygous	119989562
X	21733346	21733347	G	A	31	GENIC	possibly homozygous	108238332
X	21735344	21735345	T	G	67	GENIC	possibly homozygous	108238334
X	21738745	21738746	C	T	63	GENIC	homozygous	108238336
X	21740780	21740781	T	C	68	GENIC	homozygous	108238338
X	21745358	21745359	G	A	43	GENIC	homozygous	108238340
X	21749007	21749008	C	T	83	GENIC	homozygous	108238342
X	21753921	21753922	G	A	72	GENIC	heterozygous	119909803
X	21738764	21738765	C	T	67	GENIC	homozygous	108439628