chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221256714221256715TA23GENIChomozygous108994673
1221258596221258597CA23GENIChomozygous108994674
1221258654221258655AG21GENIChomozygous108544177
1221259850221259851TC18GENIChomozygous108544185
1221260231221260232TC25GENIChomozygous108544187
1221261019221261020GT29GENIChomozygous108544193
1221261473221261474TC15GENIChomozygous108544195
1221261583221261584GA25GENIChomozygous108994675
1221262666221262667CG25GENIChomozygous108544201
1221262951221262952GA28GENIChomozygous108994676
1221263279221263280CT30GENIChomozygous108544206
1221263389221263390TC14GENIChomozygous108544208
1221263468221263469CT25GENICpossibly homozygous108994677
1221264513221264514TC35GENIChomozygous108544210
1221264559221264560GA37GENIChomozygous108994678
1221264851221264852AC25GENICheterozygous108994679
1221264862221264863AC25GENICheterozygous108994680
1221265287221265288AG26GENIChomozygous108544216
1221266659221266660GA19GENIChomozygous108994681
1221267132221267133GC26GENIChomozygous108994682
1221267506221267507GA27GENIChomozygous108994683
1221268701221268702AG4GENIChomozygous108544238