chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	112020171	112020172	G		9	GENIC	homozygous	129780123
X	112039162	112039162		G	5	GENIC	homozygous	132251889
X	112039182	112039182		T	4	GENIC	homozygous	129780124
X	112042416	112042416		C	16	GENIC	homozygous	129780125
X	112071201	112071201		T	9	GENIC	homozygous	129780126
X	112093974	112093977	AAA		13	GENIC	homozygous	129780128
X	112108358	112108358		A	14	GENIC	homozygous	129780129
X	112108370	112108370		A	13	GENIC	homozygous	129780130
X	112108437	112108437		TTTC	9	GENIC	homozygous	129780131
X	112108440	112108445	TTAAA		10	GENIC	homozygous	129780132
X	112108511	112108511		ATACT	10	GENIC	homozygous	129780133
X	112108514	112108516	AA		13	GENIC	homozygous	129780134
X	112058267	112058268	T	C	10	GENIC	homozygous	108552688
X	112108516	112108517	A	T	13	GENIC	homozygous	108418146
X	112108235	112108236	G	T	9	GENIC	homozygous	108308892
X	112108247	112108248	G	T	7	GENIC	homozygous	108308894
X	112108445	112108446	A	C	10	GENIC	homozygous	108308900
X	112116573	112116574	T	G	7	GENIC	possibly homozygous	108308902