chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	40463728	40463729	A	T	3	GENIC	homozygous	108256750
X	40469903	40469904	A	G	6	GENIC	homozygous	108256752
X	40506927	40506928	C	T	6	GENIC	homozygous	108566701
X	40506929	40506930	T	C	6	GENIC	homozygous	108566703
X	40506950	40506951	A	G	7	GENIC	homozygous	108566705
X	40506975	40506976	C	T	8	GENIC	homozygous	108566707
X	40509800	40509801	T	A	3	GENIC	homozygous	108256760
X	40566382	40566383	G	T	5	GENIC	homozygous	108256774
X	40566505	40566506	G	A	9	GENIC	homozygous	108256777
X	40566513	40566514	T	A	11	GENIC	homozygous	108256779
X	40566515	40566516	A	T	12	GENIC	homozygous	108256781
X	40631666	40631667	T	C	10	GENIC	homozygous	108256783
X	40645242	40645243	T	G	6	GENIC	homozygous	108256789
X	40646828	40646829	A	T	3	GENIC	homozygous	108766545
X	40646829	40646830	C	A	3	GENIC	homozygous	108766548
X	40646833	40646834	T	G	3	GENIC	homozygous	108766550
X	40684932	40684933	C	T	7	GENIC	homozygous	108256791
X	40684935	40684936	C	T	7	GENIC	homozygous	108256793
X	40687317	40687318	T	G	7	GENIC	homozygous	108256795
X	40703458	40703459	G	T	15	GENIC	homozygous	108256797
X	40703482	40703483	G	T	12	GENIC	homozygous	108256799
X	40632025	40632026	C	A	5	GENIC	homozygous	108446458
X	40526333	40526334	A	T	2	GENIC	homozygous	108380422
X	40526335	40526336	A	C	2	GENIC	homozygous	108380424