chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72564288025642881AG53GENIChomozygous138041379
72564293025642931GA56GENIChomozygous144785172
72564413025644131AC61GENIChomozygous138041380
72564546925645470AG36GENIChomozygous138041381
72564631525646316GC60GENIChomozygous138041382
72564790125647902CT51GENIChomozygous144785173
72564551125645512GA27GENIChomozygous403205042
72564551125645512G27GENICheterozygous403205043
72564890325648904GT33GENIChomozygous138041385
72564977725649778AT53GENIChomozygous138041386
72565230925652310CT39GENIChomozygous144785174
72565321525653216TC56GENICpossibly homozygous138041388
72565345625653457GA55GENIChomozygous144785175
72565358225653583CA52GENIChomozygous138041389
72565461425654615GC66GENICpossibly homozygous138041390
72566049425660495AG48GENIChomozygous144785177
72565131225651314TT23GENIChomozygous144778280
72565282525652825G21GENICheterozygous144778281
72565580325655804GA61GENIChomozygous138041391
72565679025656791GA49GENIChomozygous144785176
72565789925657900AG52GENIChomozygous138041394
72566080225660803GA53GENIChomozygous144785178
72566209425662095TC70GENIChomozygous138041396
72566350025663501AG62GENICpossibly homozygous138041397
72566400525664006CT44GENIChomozygous144785179
72566597025665971GA44GENIChomozygous144785180
72566634725666348AG43GENIChomozygous138041401