chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	75979962	75979963	A	G	23	GENIC	homozygous	185298678
4	75979980	75979981	G	A	19	GENIC	homozygous	187141257
4	75981381	75981382	A	T	7	GENIC	heterozygous	187141258
4	75981999	75982000	G	A	17	GENIC	homozygous	187141259
4	75982493	75982494	T	G	15	GENIC	homozygous	187141260
4	75983865	75983866	A	C	19	GENIC	homozygous	187141261
4	75984901	75984902	A	G	19	GENIC	homozygous	185298679
4	75986298	75986299	G	A	21	GENIC	homozygous	187141262
4	75988564	75988565	G	A	11	GENIC	homozygous	185298680
4	75989131	75989132	G	T	18	GENIC	possibly homozygous	185298681
4	75989792	75989793	C	T	19	GENIC	homozygous	187141263
4	75990407	75990408	G	T	11	GENIC	homozygous	187141264
4	75991343	75991344	A	T	13	GENIC	homozygous	185298682
4	75994041	75994042	A	G	19	GENIC	homozygous	185298683
4	75996004	75996005	A	G	15	GENIC	homozygous	185298684
4	75996005	75996006	T	A	16	GENIC	homozygous	185298685
4	75996374	75996375	A	G	17	GENIC	homozygous	185298686
4	75996829	75996830	C	T	3	GENIC	homozygous	187141265
4	75996982	75996983	G	C	3	GENIC	homozygous	187141266
4	75999200	75999201	A	G	19	GENIC	homozygous	187141267
4	76000538	76000539	C	T	20	GENIC	homozygous	187141268
4	76001474	76001475	T	A	5	GENIC	homozygous	185298687
4	76001478	76001479	T	C	3	GENIC	homozygous	185298688
4	76001494	76001495	T	A	6	GENIC	homozygous	185298689
4	76001538	76001539	T	G	13	GENIC	homozygous	185298690
4	76001540	76001541	C	T	11	GENIC	homozygous	185298691
4	76001602	76001603	A	C	7	GENIC	homozygous	185298692
4	76001646	76001647	A	G	4	GENIC	homozygous	187141269
4	76001650	76001651	A	C	5	GENIC	homozygous	185298693