chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	54040383	54040384	A	G	4	GENIC	homozygous	108498296
X	54041035	54041036	T	C	3	GENIC	homozygous	108795235
X	54050520	54050521	C	T	6	GENIC	homozygous	108264929
X	54050782	54050783	A	C	4	GENIC	homozygous	108264931
X	54052622	54052623	C	T	3	GENIC	homozygous	108381757
X	54059368	54059369	C	T	3	GENIC	homozygous	108264933
X	54059691	54059692	C	G	4	GENIC	homozygous	108264935
X	54060636	54060637	T	G	4	GENIC	homozygous	108264937
X	54060908	54060909	A	T	8	GENIC	homozygous	108264939
X	54060920	54060921	G	C	7	GENIC	homozygous	108264941
X	54061534	54061535	C	G	6	GENIC	homozygous	108264943
X	54061887	54061888	C	T	5	GENIC	homozygous	108264945
X	54062466	54062467	C	G	3	GENIC	homozygous	108264947
X	54062646	54062647	G	T	3	GENIC	homozygous	108264949
X	54064141	54064142	G	C	3	GENIC	homozygous	108264951
X	54064993	54064994	G	A	2	GENIC	homozygous	108264953
X	54065306	54065307	T	G	5	GENIC	homozygous	108264955
X	54065341	54065342	A	G	4	GENIC	homozygous	108264957
X	54070198	54070199	C	T	8	GENIC	homozygous	108264961
X	54069752	54069753	G	T	2	GENIC	homozygous	108820019
X	54069767	54069768	G	T	2	GENIC	homozygous	108551345
X	54084432	54084433	T	C	3	GENIC	homozygous	108526240
X	54084705	54084706	G	C	2	GENIC	homozygous	108264971
X	54085291	54085292	A	G	3	GENIC	homozygous	108264973