chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	45379405	45379406	A	AT	24	GENIC	homozygous	45127646
X	45379514	45379515	C	-	28	GENIC	homozygous	45127647
X	45379519	45379520	A	AG	32	GENIC	homozygous	45127648
X	45392559	45392560	A	G	51	GENIC	heterozygous	45127649
X	45392584	45392585	C	A	52	GENIC	heterozygous	45127650
X	45392608	45392609	G	A	48	GENIC	heterozygous	45127651
X	45399228	45399229	T	G	21	GENIC	heterozygous	45127652
X	45400463	45400464	C	-	7	GENIC	homozygous	45127653
X	45406431	45406432	T	TTATCTATC	8	GENIC	possibly homozygous	45127654
X	45407643	45407644	G	A	22	GENIC	heterozygous	45127655
X	45407676	45407677	A	-	13	GENIC	heterozygous	45127656
X	45409624	45409628	CTAG	----	17	GENIC	homozygous	45127657
X	45417804	45417805	T	TA	2	GENIC	homozygous	45127658
X	45417811	45417812	C	CTATA	3	GENIC	homozygous	45127659
X	45418144	45418145	C	CCAG	15	GENIC	homozygous	45127660
X	45418270	45418271	A	AG	4	GENIC	homozygous	45127661