chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134346554043465541CT34GENIChomozygous115008988
134346557743465578TC35GENIChomozygous118496653
134346621443466215CT15GENIChomozygous115008990
134346638543466386TC27GENIChomozygous115008992
134346644143466442GA30GENIChomozygous115008994
134346668243466683GT31GENIChomozygous115008996
134346728543467286TC24GENIChomozygous114544339
134346739643467397CG18GENIChomozygous115008998
134346740243467403AG17GENIChomozygous114544341
134346841343468414CT24GENICpossibly homozygous115009000
134346846743468468CT21GENICheterozygous118496654
134346848743468488CA23GENICheterozygous118496655
134346849243468493GA24GENICheterozygous118496656
134346890043468901GA27GENIChomozygous115009002
134346893343468934GC21GENIChomozygous114544347
134346800943468010AG22GENIChomozygous114544343
134346889943468900TC26GENIChomozygous114544345
134346843743468438TC22GENICheterozygous118566577
134346843943468440CA22GENICheterozygous118566578
134346906343469064AT27GENIChomozygous114544349
134346911543469116AG24GENIChomozygous114544351
134347140243471403TC30GENIChomozygous115009004
134347325043473251AG43GENIChomozygous115009006
134347361743473618AG35GENIChomozygous114544359
134347468243474683AG31GENIChomozygous114544363
134347544043475441GA22GENIChomozygous115009008
134347544343475444CT23GENIChomozygous115009010
134347587943475880TC33GENIChomozygous114544369
134347208343472084CT34GENICheterozygous115217787