chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
470897097089710AG13GENIChomozygous58059348
470903497090350AACTTTATATTTCTAC2GENIChomozygous57416049
470904437090444GA25GENICpossibly homozygous58059350
470920557092056AG4GENIChomozygous57416059
470929637092964TG20GENIChomozygous57416067
470933547093355AG17GENICpossibly homozygous57416069
470941557094156TA10GENIChomozygous58059352
470942787094279AG2GENIChomozygous58059354
470957397095740GA25GENICpossibly homozygous58059356
470958617095862CT14GENICpossibly homozygous58059358
470963137096314TC18GENIChomozygous57416085
470965027096503GA3GENICheterozygous58059360
470967877096788TC14GENIChomozygous57416087
470975087097509G-22GENIChomozygous58059362
470993057099306GT19GENIChomozygous58059366
471003387100339TC12GENIChomozygous58059368
471004917100492TC16GENIChomozygous57416095
471017457101755AGGACAGGAC----------1GENIChomozygous57416099
471020847102085TC12GENICpossibly homozygous57416101
471026227102623GA24GENICpossibly homozygous58059370
471034237103424TC24GENICpossibly homozygous57416107
471047037104704AG17GENIChomozygous58059376
471055537105554GGAAC6GENICheterozygous58059378
471059577105958CT31GENICpossibly homozygous58059380
471061017106102CT21GENICheterozygous58059382
471074437107444GA7GENICheterozygous58059384
471081727108173CT8GENICheterozygous58059386
471087037108704GA7GENIChomozygous57416116
471092797109280AG22GENICpossibly homozygous58059388
471097277109728TTCCAGCCA5GENIChomozygous58059390
471129337112934TG23GENIChomozygous57416128
471131367113137GT12GENICpossibly homozygous58059396
471138477113848GA27GENICpossibly homozygous58059398
471144407114441CG2GENICheterozygous58059400
471150987115099CT24GENICpossibly homozygous58059402
471169527116953GA26GENIChomozygous58059404
471187187118719GA20GENICpossibly homozygous58059406
470934907093491CCGCAG2GENIChomozygous58861732
471078887107889AAC5GENICheterozygous56736193