chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	59665655	59665656	C	G	22	GENIC	homozygous	111583944
3	59666533	59666534	C	T	31	GENIC	homozygous	111583945
3	59667198	59667199	A	G	17	GENIC	homozygous	112384727
3	59667982	59667983	T	A	31	GENIC	homozygous	111583948
3	59669416	59669417	A	G	31	GENIC	homozygous	111583949
3	59672106	59672107	G	A	14	GENIC	homozygous	111583950
3	59676917	59676918	A	G	35	GENIC	homozygous	111583951
3	59679100	59679101	C	T	30	GENIC	homozygous	111583952
3	59680342	59680343	C	T	25	GENIC	homozygous	111583953
3	59682062	59682063	A	T	35	GENIC	homozygous	111583954
3	59682703	59682704	A	T	32	GENIC	homozygous	111583955
3	59683340	59683341	A	G	25	GENIC	homozygous	111583956
3	59683621	59683622	T	A	18	GENIC	homozygous	111583957
3	59683854	59683855	G	A	15	GENIC	homozygous	111583958
3	59684031	59684032	T	G	3	GENIC	homozygous	111911041
3	59684924	59684925	T	C	42	GENIC	homozygous	111583960
3	59685652	59685653	C	T	35	GENIC	possibly homozygous	111583961
3	59686076	59686077	T	G	22	GENIC	homozygous	111583962
3	59686088	59686089	T	G	24	GENIC	homozygous	111583963
3	59686754	59686755	G	A	38	GENIC	homozygous	111583964