chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	71218092	71218093	T		1	GENIC	homozygous	129753925
X	71218097	71218098	G		1	GENIC	homozygous	129753926
X	71218107	71218108	G	C	1	GENIC	homozygous	129817469
X	71218110	71218111	G		1	GENIC	homozygous	129753927
X	71218117	71218118	C		1	GENIC	homozygous	129753928
X	71218123	71218124	C		1	GENIC	homozygous	129753929
X	71218128	71218131	GAG		1	GENIC	homozygous	129753930
X	71218133	71218134	G		1	GENIC	homozygous	129753931
X	71218135	71218136	C	T	1	GENIC	homozygous	108677230
X	71218142	71218142		C	1	GENIC	homozygous	129753932
X	71218144	71218145	G		1	GENIC	homozygous	129753933
X	71218146	71218148	AG		1	GENIC	homozygous	129753934
X	71218159	71218161	TG		1	GENIC	homozygous	129753935
X	71218166	71218167	G		1	GENIC	homozygous	129753936
X	71218168	71218169	G		1	GENIC	homozygous	129753937
X	71218175	71218175		C	1	GENIC	homozygous	129753938
X	71218225	71218226	C	G	2	GENIC	homozygous	108391239
X	71218226	71218227	G	C	2	GENIC	homozygous	108391241
X	71218234	71218238	GCCG		2	GENIC	homozygous	129753939
X	71218238	71218239	C	T	3	GENIC	homozygous	108391243
X	71218257	71218257		T	4	GENIC	homozygous	129753940
X	71218314	71218315	C		11	GENIC	homozygous	129753941
X	71218323	71218324	G		11	GENIC	homozygous	129753942
X	71218350	71218351	C		11	GENIC	homozygous	129753943