chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115639594	115639595	C	T	7	GENIC	homozygous	108312640
X	115639851	115639852	A	C	6	GENIC	homozygous	108312644
X	115640075	115640076	T	G	7	GENIC	homozygous	108312646
X	115666331	115666332	G	A	4	GENIC	homozygous	108312650
X	115672727	115672728	G	A	6	GENIC	homozygous	108312656
X	115672728	115672729	T	C	6	GENIC	homozygous	108312658
X	115672729	115672730	G	T	6	GENIC	homozygous	108312660
X	115672738	115672739	G	C	5	GENIC	homozygous	108312662
X	115672741	115672742	T	C	5	GENIC	homozygous	108312664
X	115672745	115672746	G	A	3	GENIC	homozygous	108312666
X	115761816	115761817	A	T	7	GENIC	homozygous	108312676
X	115761817	115761818	T	A	7	GENIC	homozygous	108312678
X	115769214	115769215	C	G	5	GENIC	homozygous	108529804
X	115774512	115774513	G	C	14	GENIC	homozygous	108312680
X	115866973	115866974	A	C	4	GENIC	homozygous	108312682
X	115866976	115866977	A	G	4	GENIC	homozygous	108312684
X	115866979	115866980	A	T	4	GENIC	homozygous	108312686
X	115866980	115866981	A	C	4	GENIC	homozygous	108312688
X	115826147	115826148	T	C	6	GENIC	homozygous	108687949
X	115903272	115903273	A	T	10	GENIC	homozygous	108687951