chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34632800646328007AG13GENIChomozygous885766609
34632844746328448CA8GENICheterozygous885766610
34632846146328462AT10GENICheterozygous885766611
34632878946328790CT26GENIChomozygous885766612
34632894746328948CT20GENIChomozygous885766613
34632896346328964AG15GENICheterozygous885766614
34632946946329470GT16GENIChomozygous885766615
34633021546330216TA20GENIChomozygous885766616
34633045446330455GA17GENIChomozygous885766617
34633095346330954GA16GENIChomozygous885766618
34633115346331154AG30GENIChomozygous885766619
34633631246336313TC20GENIChomozygous885766620
34633638346336384TG26GENIChomozygous885766621
34633742646337427AC19GENIChomozygous885766622
34633904246339043AG22GENIChomozygous885766623
34633938046339381TC12GENIChomozygous885766624
34634092946340930CT12GENIChomozygous885766625
34634136046341361CT25GENIChomozygous885766626
34634192146341922AG15GENIChomozygous885766627
34634200946342010GT24GENIChomozygous885766628
34634218446342185TC15GENIChomozygous885766629
34634448746344488AT18GENIChomozygous885766630
34634656446346565AG17GENIChomozygous885766631
34634845946348460TC16GENIChomozygous885766632
34634973746349738AG21GENICpossibly homozygous885766633
34634998246349983TA8GENIChomozygous885766634
34635100646351007AG8GENIChomozygous885766635
34635180346351804TC12GENIChomozygous885766636
34635198746351988CG18GENIChomozygous885766637
34635198846351989AT19GENIChomozygous885766638
34635456446354565TA5GENIChomozygous885766639
34635791146357912GA23GENIChomozygous885766640
34635826746358268CT21GENIChomozygous885766641
34636006946360070GC6GENICheterozygous885766642