chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	112020171	112020172	G		12	GENIC	homozygous	129780123
X	112039182	112039182		T	6	GENIC	homozygous	129780124
X	112042416	112042416		C	23	GENIC	homozygous	129780125
X	112071201	112071201		T	18	GENIC	homozygous	129780126
X	112080989	112080989		TC	10	GENIC	homozygous	129780127
X	112093974	112093977	AAA		17	GENIC	homozygous	129780128
X	112108358	112108358		A	21	GENIC	homozygous	129780129
X	112108370	112108370		A	16	GENIC	homozygous	129780130
X	112108437	112108437		TTTC	15	GENIC	homozygous	129780131
X	112108440	112108445	TTAAA		16	GENIC	homozygous	129780132
X	112108511	112108511		ATACT	13	GENIC	homozygous	129780133
X	112108514	112108516	AA		13	GENIC	homozygous	129780134
X	112108516	112108517	A	T	13	GENIC	homozygous	108418146
X	112108267	112108268	G	A	24	GENIC	homozygous	108308896
X	112058267	112058268	T	C	18	GENIC	homozygous	108552688
X	112108235	112108236	G	T	21	GENIC	homozygous	108308892
X	112108247	112108248	G	T	22	GENIC	homozygous	108308894
X	112108271	112108272	G	T	24	GENIC	homozygous	108308898
X	112108445	112108446	A	C	16	GENIC	homozygous	108308900
X	112116573	112116574	T	G	20	GENIC	possibly homozygous	108308902