chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	54069976	54069977	G	T	22	GENIC	homozygous	108264959
X	54083060	54083061	A	T	11	GENIC	homozygous	108498306
X	54083070	54083071	G	T	11	GENIC	homozygous	108446842
X	54083085	54083086	C	T	10	GENIC	homozygous	108446844
X	54083088	54083089	A	T	9	GENIC	homozygous	108446846
X	54083096	54083097	G	T	11	GENIC	homozygous	108446848
X	54083106	54083107	A	T	9	GENIC	homozygous	108446850
X	54083111	54083112	C	T	11	GENIC	homozygous	108446852
X	54083126	54083127	C	A	13	GENIC	homozygous	108446854
X	54083132	54083133	G	T	14	GENIC	homozygous	108446856
X	54083236	54083237	C	T	10	GENIC	homozygous	108264963
X	54083242	54083243	G	C	10	GENIC	homozygous	108264965
X	54083269	54083270	A	C	7	GENIC	homozygous	108264967
X	54083275	54083276	G	C	8	GENIC	homozygous	108264969
X	54083291	54083292	A	C	7	GENIC	homozygous	108446858