chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115639594	115639595	C	T	19	GENIC	homozygous	108312640
X	115639829	115639830	C	T	17	GENIC	homozygous	108312642
X	115639851	115639852	A	C	13	GENIC	homozygous	108312644
X	115640075	115640076	T	G	22	GENIC	homozygous	108312646
X	115666331	115666332	G	A	16	GENIC	homozygous	108312650
X	115672777	115672778	G	T	19	GENIC	homozygous	108312668
X	115672783	115672784	G	T	22	GENIC	homozygous	108312670
X	115761816	115761817	A	T	28	GENIC	homozygous	108312676
X	115761817	115761818	T	A	28	GENIC	homozygous	108312678
X	115866973	115866974	A	C	9	GENIC	homozygous	108312682
X	115866976	115866977	A	G	8	GENIC	homozygous	108312684
X	115866979	115866980	A	T	8	GENIC	homozygous	108312686
X	115866980	115866981	A	C	8	GENIC	homozygous	108312688