chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7134058771134058772TC15GENIChomozygous142016286
7134058828134058829TG17GENIChomozygous142016287
7134059397134059397CG27GENICpossibly homozygous141924562
7134059399134059399GCCGCCG27GENICpossibly homozygous141924563
7134059688134059689GA27GENIChomozygous142016288
7134060113134060114AG52GENIChomozygous142016289
7134061277134061278AG55GENIChomozygous142016290
7134061861134061862GA43GENIChomozygous142016291
7134062121134062122GA57GENIChomozygous142016292
7134062160134062161GA54GENIChomozygous142016293
7134062235134062236GA54GENIChomozygous142016294
7134062513134062513G45GENIChomozygous141924564
7134062622134062623GT60GENIChomozygous142016295
7134062969134062969A51GENIChomozygous137985411
7134063298134063299GT61GENIChomozygous142016296
7134063322134063323G59GENICheterozygous149353970
7134063322134063323GA59GENIChomozygous154486060
7134063391134063392AT45GENIChomozygous142016297
7134063516134063517AT60GENIChomozygous142016298
7134063534134063535TA65GENIChomozygous142016299
7134063702134063702T52GENICpossibly homozygous141924565
7134065032134065033CT51GENIChomozygous142016300
7134065346134065347CT25GENICpossibly homozygous142016301
7134063934134063935AG60GENIChomozygous138229766
7134061757134061758C16GENICheterozygous403228225
7134061757134061758CT16GENICheterozygous403228226
7134061808134061809A12GENICheterozygous403618611
7134061808134061809AT12GENICheterozygous403618612
7134065454134065456CC3GENIChomozygous137985412