chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	74618556	74618557	G	A	10	GENIC	homozygous	108274798
X	74618557	74618558	T	G	10	GENIC	homozygous	108274800
X	74618793	74618794	G	T	13	GENIC	homozygous	108274802
X	74618872	74618873	T	G	17	GENIC	homozygous	108274804
X	74650285	74650286	T	G	8	GENIC	homozygous	108391547
X	74650410	74650411	G	A	13	GENIC	homozygous	108391551
X	74650415	74650416	G	A	12	GENIC	homozygous	108274806
X	74650472	74650473	G	A	10	GENIC	homozygous	108391553
X	74651043	74651044	G	T	4	GENIC	homozygous	108274808
X	74651044	74651045	T	G	4	GENIC	homozygous	108274810
X	74651052	74651053	T	G	4	GENIC	homozygous	108274812
X	74651053	74651054	G	T	5	GENIC	homozygous	108274814
X	74651356	74651357	T	C	8	GENIC	homozygous	108274816