chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	7376704	7376705	C	G	9	GENIC	homozygous	45082710
X	7377492	7377493	G	A	11	GENIC	homozygous	45082711
X	7380941	7380942	T	TA	10	GENIC	homozygous	45082712
X	7389369	7389370	T	TC	9	GENIC	homozygous	45082715
X	7395973	7395974	A	T	12	GENIC	homozygous	45082722
X	7403400	7403401	T	-	10	GENIC	homozygous	45082729
X	7403896	7403897	A	-	10	GENIC	homozygous	45082730
X	7404024	7404025	T	C	8	GENIC	homozygous	45082731
X	7407709	7407710	G	A	7	GENIC	homozygous	45082737
X	7407858	7407859	T	-	7	GENIC	homozygous	45082738
X	7416942	7416943	C	T	10	GENIC	homozygous	45082740
X	7420680	7420681	G	T	10	GENIC	homozygous	45082741
X	7420686	7420687	G	T	10	GENIC	homozygous	45082742
X	7420690	7420691	T	-	10	GENIC	homozygous	45082743
X	7425654	7425655	C	-	7	GENIC	homozygous	45082744
X	7433665	7433666	T	-	13	GENIC	homozygous	45082746