chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	110903046	110903047	A	T	11	GENIC	homozygous	108308755
X	110903049	110903050	T	A	11	GENIC	homozygous	108308757
X	110903269	110903270	G	A	23	GENIC	homozygous	108506880
X	110903511	110903512	G	C	15	GENIC	homozygous	108308759
X	110906891	110906892	C	T	23	GENIC	homozygous	108308761
X	110906892	110906893	C	T	23	GENIC	homozygous	108308763
X	110911116	110911117	C	A	18	GENIC	homozygous	108308765
X	110932836	110932837	G	A	3	GENIC	homozygous	108416603
X	110932839	110932840	C	A	3	GENIC	homozygous	108416605
X	110932845	110932846	C	G	3	GENIC	homozygous	108598715
X	110932849	110932850	C	G	3	GENIC	homozygous	108779646
X	110932855	110932856	C	T	3	GENIC	homozygous	108779648
X	110932864	110932865	A	G	1	GENIC	homozygous	108779650
X	110940136	110940137	G	T	10	GENIC	homozygous	108308767
X	110940211	110940212	G	A	7	GENIC	homozygous	108308769
X	110957382	110957383	T	A	14	GENIC	homozygous	108308771
X	110957386	110957387	A	T	14	GENIC	homozygous	108308773