chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34632746746327468GA19GENIChomozygous802384961
34632800646328007AG14GENIChomozygous802384962
34632844746328448CA22GENIChomozygous802384963
34632878946328790CT22GENIChomozygous802384964
34632894746328948CT20GENIChomozygous802384965
34632896346328964AG21GENIChomozygous802384966
34632946946329470GT18GENIChomozygous802384967
34633021546330216TA19GENIChomozygous802384968
34633045446330455GA12GENIChomozygous802384969
34633095346330954GA11GENIChomozygous802384970
34633115346331154AG26GENIChomozygous802384971
34633631246336313TC24GENIChomozygous802384972
34633638346336384TG18GENIChomozygous802384973
34633742646337427AC16GENIChomozygous802384974
34633904246339043AG19GENIChomozygous802384975
34633938046339381TC14GENIChomozygous802384976
34634092946340930CT27GENICpossibly homozygous802384977
34634136046341361CT10GENIChomozygous802384978
34634192146341922AG12GENIChomozygous802384979
34634200946342010GT15GENIChomozygous802384980
34634218446342185TC18GENIChomozygous802384981
34634448746344488AT17GENIChomozygous802384982
34634632146346322CT13GENIChomozygous802384983
34634656446346565AG21GENIChomozygous802384984
34634845946348460TC8GENIChomozygous802384985
34634864846348649TA8GENIChomozygous802384986
34634973746349738AG36GENIChomozygous802384987
34634998246349983TA15GENIChomozygous802384988
34635100646351007AG21GENIChomozygous802384989
34635180346351804TC17GENIChomozygous802384990
34635198746351988CG18GENIChomozygous802384991
34635198846351989AT18GENIChomozygous802384992
34635206546352066AC23GENICheterozygous802384993
34635207146352072TC23GENICheterozygous802384994
34635456446354565TA18GENICpossibly homozygous802384995
34635791146357912GA21GENIChomozygous802384996
34635826746358268CT22GENIChomozygous802384997