chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115110979	115110980	C	T	11	GENIC	homozygous	108312597
X	115114038	115114039	G		5	GENIC	homozygous	129781898
X	115139619	115139621	CT		18	GENIC	heterozygous	132927432
X	115147967	115147968	C		9	GENIC	homozygous	129781899
X	115147977	115147978	C		9	GENIC	homozygous	129781900
X	115147979	115147980	C		7	GENIC	homozygous	129781901
X	115147986	115147987	C		7	GENIC	homozygous	129781902
X	115147992	115147992		T	7	GENIC	homozygous	129781903
X	115147999	115148000	C		7	GENIC	homozygous	129781904
X	115148006	115148007	C		9	GENIC	homozygous	129781905
X	115148014	115148014		A	9	GENIC	homozygous	129781906
X	115148043	115148045	AT		13	GENIC	homozygous	129781907
X	115154941	115154941		T	12	GENIC	homozygous	129781916
X	115147949	115147950	T	G	9	GENIC	homozygous	108552730
X	115147950	115147951	C	T	9	GENIC	homozygous	108552732
X	115149153	115149154	A	C	8	GENIC	homozygous	108419362