chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115639594	115639595	C	T	8	GENIC	homozygous	108312640
X	115639829	115639830	C	T	13	GENIC	homozygous	108312642
X	115639851	115639852	A	C	14	GENIC	homozygous	108312644
X	115640075	115640076	T	G	10	GENIC	homozygous	108312646
X	115666331	115666332	G	A	14	GENIC	homozygous	108312650
X	115672705	115672706	G	T	11	GENIC	homozygous	108312652
X	115672720	115672721	A	G	8	GENIC	homozygous	108312654
X	115672727	115672728	G	A	9	GENIC	homozygous	108312656
X	115672728	115672729	T	C	9	GENIC	homozygous	108312658
X	115672738	115672739	G	C	8	GENIC	homozygous	108312662
X	115672741	115672742	T	C	8	GENIC	homozygous	108312664
X	115672745	115672746	G	A	8	GENIC	homozygous	108312666
X	115672777	115672778	G	T	9	GENIC	homozygous	108312668
X	115672783	115672784	G	T	11	GENIC	homozygous	108312670
X	115761816	115761817	A	T	10	GENIC	homozygous	108312676
X	115761817	115761818	T	A	10	GENIC	homozygous	108312678
X	115774512	115774513	G	C	22	GENIC	homozygous	108312680
X	115840240	115840241	C	T	19	GENIC	homozygous	108635149
X	115866973	115866974	A	C	10	GENIC	homozygous	108312682