chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	112999028	112999029	C	T	29	GENIC	heterozygous	45311720
X	112999210	112999211	T	C	21	GENIC	heterozygous	45311721
X	112999603	112999604	A	G	18	GENIC	heterozygous	45311722
X	112999604	112999605	A	C	17	GENIC	heterozygous	45311723
X	112999606	112999607	A	C	17	GENIC	heterozygous	45311724
X	113000158	113000159	A	AGG	10	GENIC	heterozygous	45889035
X	113000160	113000168	TGCCTCAA	--------	8	GENIC	heterozygous	45889036
X	113000254	113000255	C	T	12	GENIC	heterozygous	45311725
X	113000515	113000516	C	T	6	GENIC	heterozygous	45889037
X	113004408	113004409	A	C	7	GENIC	heterozygous	45595062
X	113004409	113004410	C	T	7	GENIC	heterozygous	45595064
X	113022945	113022946	C	T	20	GENIC	heterozygous	45889042
X	113029693	113029694	T	-	23	GENIC	heterozygous	45889050
X	113035560	113035561	T	C	18	GENIC	heterozygous	45311825
X	113058188	113058189	A	-	11	GENIC	heterozygous	45889082
X	113069669	113069670	A	-	13	GENIC	heterozygous	45858878
X	113074605	113074606	A	ACTTC	13	GENIC	heterozygous	45889108
X	113097911	113097912	C	CT	8	GENIC	heterozygous	45889142
X	113100858	113100859	C	T	19	GENIC	heterozygous	45854487