chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	40463728	40463729	A	T	6	GENIC	homozygous	108256750
X	40469903	40469904	A	G	33	GENIC	homozygous	108256752
X	40509800	40509801	T	A	20	GENIC	homozygous	108256760
X	40566382	40566383	G	T	26	GENIC	homozygous	108256774
X	40566505	40566506	G	A	19	GENIC	homozygous	108256777
X	40566513	40566514	T	A	18	GENIC	homozygous	108256779
X	40566515	40566516	A	T	18	GENIC	homozygous	108256781
X	40567824	40567825	C	G	2	GENIC	homozygous	108446454
X	40568040	40568041	A	T	10	GENIC	homozygous	108446456
X	40631666	40631667	T	C	21	GENIC	homozygous	108256783
X	40645242	40645243	T	G	6	GENIC	homozygous	108256789
X	40684932	40684933	C	T	24	GENIC	homozygous	108256791
X	40684935	40684936	C	T	23	GENIC	homozygous	108256793
X	40687317	40687318	T	G	19	GENIC	homozygous	108256795
X	40703458	40703459	G	T	26	GENIC	homozygous	108256797
X	40703482	40703483	G	T	27	GENIC	homozygous	108256799