chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141852210718522108TC19GENIChomozygous113366510
141852231718522318TC7GENIChomozygous113366512
141852235618522357TC3GENIChomozygous113810339
141852259018522591CA12GENIChomozygous113366514
141852265718522658GT24GENICpossibly homozygous113366516
141852266418522665AG22GENICpossibly homozygous114096929
141852267318522674CT23GENIChomozygous113366518
141852268118522682GA23GENIChomozygous113366520
141852274418522745CT22GENIChomozygous113366522
141852288218522883GA26GENIChomozygous113366524
141852289218522893CT25GENIChomozygous113366526
141852303718523038AT32GENIChomozygous113366530
141852305418523055AG34GENIChomozygous113366532
141852329918523300CT29GENIChomozygous113366534
141852413118524132CT24GENIChomozygous113810341
141852490718524908AG21GENICpossibly homozygous113810345
141852566318525664CT24GENICpossibly homozygous113810347
141852585318525854AG33GENIChomozygous113366536
141852840818528409AG37GENIChomozygous113366538
141852883518528836GA27GENIChomozygous113810349
141852453518524536GC23GENIChomozygous113664097
141852939018529391AG23GENIChomozygous113366540
141852954018529541GA25GENIChomozygous113366547
141853028718530288GA27GENICpossibly homozygous113664105
141853039218530393GA19GENICpossibly homozygous113810351
141853070818530709AG27GENIChomozygous113366551