chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	112999210	112999211	T	C	22	GENIC	heterozygous	45311721
X	112999362	112999363	C	T	27	GENIC	heterozygous	46019028
X	112999603	112999604	A	G	18	GENIC	heterozygous	45311722
X	112999604	112999605	A	C	18	GENIC	heterozygous	45311723
X	112999606	112999607	A	C	18	GENIC	heterozygous	45311724
X	113000091	113000092	T	C	11	GENIC	heterozygous	46019029
X	113000254	113000255	C	T	29	GENIC	heterozygous	45311725
X	113008352	113008353	T	G	12	GENIC	heterozygous	45311738
X	113015840	113015841	A	T	12	GENIC	heterozygous	45311763
X	113016175	113016176	C	CA	11	GENIC	heterozygous	46019030
X	113016983	113016984	G	A	10	GENIC	heterozygous	45311766
X	113017590	113017591	A	G	18	GENIC	heterozygous	45311770
X	113017646	113017647	G	A	10	GENIC	heterozygous	45311771
X	113022882	113022883	C	-	5	GENIC	heterozygous	45311800
X	113029693	113029694	T	-	31	GENIC	heterozygous	45889050
X	113035560	113035561	T	C	18	GENIC	heterozygous	45311825
X	113048258	113048259	T	C	18	GENIC	heterozygous	46019031
X	113055792	113055793	T	C	18	GENIC	heterozygous	46019032
X	113058188	113058189	A	-	19	GENIC	heterozygous	45889082
X	113069657	113069658	C	T	14	GENIC	heterozygous	46019033