chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142129487121294872AG18GENIChomozygous187635501
142129566121295662CT8GENIChomozygous187635502
142129691421296915GA12GENIChomozygous187635503
142129763221297633CT13GENIChomozygous185122522
142129817621298177GT12GENIChomozygous187635504
142129833821298339GA13GENIChomozygous187635505
142129913821299139CT15GENIChomozygous185122523
142129924421299245AT11GENIChomozygous185122524
142129972821299729TA21GENIChomozygous187635506
142129980921299810TC29GENIChomozygous187635507
142130038721300388TC18GENIChomozygous185122525
142130154921301550GA15GENIChomozygous187635508
142130172521301726AG11GENIChomozygous185122526
142130289221302893AG18GENIChomozygous187635509
142130308421303085TC8GENICheterozygous187635510
142130309121303092GT6GENICheterozygous187635511
142130316221303163TC10GENICheterozygous187635512
142130319921303200GA7GENICheterozygous187635513
142130320421303205CT7GENICpossibly homozygous187635514
142130365821303659GA7GENICheterozygous187635515
142130366121303662AG6GENIChomozygous185122527
142130370621303707GT6GENICheterozygous187635516
142130396021303961AG9GENICheterozygous187635517
142130586321305864AG15GENIChomozygous185122528
142130606321306064TC16GENIChomozygous185122529
142130675621306757GA20GENIChomozygous187635518
142130765321307654TA12GENIChomozygous187635519
142130836221308363AT20GENIChomozygous185122530
142130840321308404GC25GENIChomozygous185122531