chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	40369741	40369742	A	G	52	GENIC	homozygous	108256738
X	40375909	40375910	C	A	35	GENIC	possibly homozygous	108256740
X	40375916	40375917	C	G	36	GENIC	possibly homozygous	108256742
X	40379863	40379864	G	C	3	GENIC	homozygous	119995545
X	40380355	40380356	T	G	14	GENIC	homozygous	119995547
X	40380370	40380371	G	T	14	GENIC	homozygous	119995549
X	40404388	40404389	G	A	58	GENIC	possibly homozygous	119995551
X	40411252	40411253	A	T	62	GENIC	homozygous	108256744
X	40380292	40380293	G	T	48	GENIC	homozygous	119917036
X	40396242	40396243	T	G	49	GENIC	homozygous	119917037
X	40400988	40400989	A	C	7	GENIC	homozygous	119917038
X	40412326	40412327	T	A	62	GENIC	heterozygous	119995553
X	40412337	40412338	G	T	59	GENIC	heterozygous	119995555
X	40412361	40412362	C	T	58	GENIC	heterozygous	119995557