chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	74618556	74618557	G	A	17	GENIC	homozygous	108274798
X	74618557	74618558	T	G	17	GENIC	homozygous	108274800
X	74618793	74618794	G	T	9	GENIC	homozygous	108274802
X	74618872	74618873	T	G	10	GENIC	homozygous	108274804
X	74647100	74647101	C	T	5	GENIC	homozygous	108501881
X	74647110	74647111	G	C	5	GENIC	homozygous	108501883
X	74650285	74650286	T	G	17	GENIC	homozygous	108391547
X	74650375	74650376	G	T	19	GENIC	homozygous	108391549
X	74650410	74650411	G	A	19	GENIC	homozygous	108391551
X	74650415	74650416	G	A	19	GENIC	homozygous	108274806
X	74650472	74650473	G	A	17	GENIC	homozygous	108391553
X	74651043	74651044	G	T	11	GENIC	homozygous	108274808
X	74651044	74651045	T	G	11	GENIC	homozygous	108274810
X	74651052	74651053	T	G	13	GENIC	homozygous	108274812
X	74651053	74651054	G	T	13	GENIC	homozygous	108274814
X	74651356	74651357	T	C	5	GENIC	homozygous	108274816
X	74651635	74651636	T	A	15	GENIC	homozygous	108391555
X	74694119	74694120	A	C	2	GENIC	homozygous	108501885