chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	64789543	64789544	G	A	40	GENIC	homozygous	113835685
5	64790852	64790853	T	C	30	GENIC	homozygous	113835686
5	64790934	64790935	A	C	30	GENIC	homozygous	113835687
5	64791602	64791603	T	A	28	GENIC	homozygous	113835688
5	64791858	64791859	G	A	27	GENIC	homozygous	113835689
5	64792353	64792354	C	T	23	GENIC	homozygous	113835690
5	64794323	64794324	C	T	20	GENIC	homozygous	113835695
5	64794679	64794680	C	T	22	GENIC	homozygous	113835696
5	64794718	64794719	A	G	20	GENIC	homozygous	113835697
5	64795355	64795356	T	C	39	GENIC	homozygous	113835698
5	64795682	64795683	A	G	26	GENIC	homozygous	113835699
5	64795909	64795910	G	A	15	GENIC	possibly homozygous	113835700
5	64796110	64796111	A	G	17	GENIC	homozygous	113835701
5	64796715	64796716	A	G	33	GENIC	homozygous	113835702
5	64796985	64796986	A	G	20	GENIC	homozygous	113835703
5	64799544	64799545	C	T	32	GENIC	homozygous	113835704
5	64799790	64799791	A	G	17	GENIC	homozygous	113835705
5	64800240	64800241	G	C	40	GENIC	homozygous	113835706
5	64795586	64795587	T	G	22	GENIC	homozygous	118843156
5	64795589	64795590	G	T	21	GENIC	homozygous	118843157