chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2051792775179278TG16GENICheterozygous63717868
2051817765181777AG24GENIChomozygous63343469
2051840855184086CT17GENICpossibly homozygous63717869
2051881885188189TC24GENIChomozygous63343474
2051888545188855AC24GENIChomozygous63343477
2051870355187036GA22GENIChomozygous63758689
2051895125189513TC13GENIChomozygous63717870
2051926405192641TG33GENIChomozygous63717871
2051956805195681GA17GENIChomozygous63717872
2051973385197339GA19GENIChomozygous63343499
2052013685201369CG17GENIChomozygous63343503
2052020395202040AG27GENIChomozygous63343505
2052057815205782AG23GENIChomozygous63343509