chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3121472959121472960CT21GENIChomozygous112296592
3121474681121474682GA19GENIChomozygous112296594
3121476562121476563CA15GENIChomozygous112296596
3121477665121477666CG9GENICheterozygous125866785
3121478191121478192CT21GENIChomozygous112296598
3121479117121479118GA9GENIChomozygous112296600
3121479307121479308TC9GENIChomozygous112296602
3121479359121479360GT15GENIChomozygous112296604
3121479819121479820AT31GENIChomozygous112296606
3121480060121480061TC19GENIChomozygous112296610
3121480351121480352GA10GENIChomozygous112296612
3121480586121480587CT20GENIChomozygous112296614
3121480816121480817CT19GENIChomozygous112296616
3121484054121484055CT16GENIChomozygous112144532
3121484389121484390CT20GENIChomozygous112296642
3121484594121484595GA10GENIChomozygous112296643
3121484612121484613AG11GENIChomozygous112296645
3121485775121485776AT17GENIChomozygous112296646
3121486492121486493AG14GENIChomozygous112296648
3121486753121486754GA17GENIChomozygous112296650
3121487737121487738AG12GENIChomozygous112144537
3121487808121487809CA6GENIChomozygous119685292
3121488503121488504CG9GENIChomozygous112296652