chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	47061104	47061105	C	A	42	GENIC	homozygous	111558433
3	47061424	47061425	T	A	21	GENIC	homozygous	111558435
3	47061541	47061542	T	C	34	GENIC	possibly homozygous	111558437
3	47061633	47061634	A	G	43	GENIC	homozygous	111558439
3	47061646	47061647	C	T	50	GENIC	homozygous	111558441
3	47061797	47061798	T	C	36	GENIC	homozygous	111558443
3	47061808	47061809	C	G	35	GENIC	homozygous	111558445
3	47061862	47061863	A	G	26	GENIC	homozygous	111558447
3	47062001	47062002	T	C	13	GENIC	heterozygous	111558449
3	47062007	47062008	T	C	10	GENIC	heterozygous	111558451
3	47062013	47062014	T	C	12	GENIC	heterozygous	111558453
3	47062248	47062249	T	C	16	GENIC	possibly homozygous	111558455
3	47062980	47062981	C	T	21	GENIC	homozygous	111558457
3	47063216	47063217	A	G	17	GENIC	homozygous	111558459
3	47063260	47063261	C	T	22	GENIC	homozygous	111558461