chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104333967104333968C22GENICheterozygous139415096
14104333972104333972A21GENICheterozygous139415097
14104334125104334125T27GENICheterozygous139415098
14104334127104334131ACAT27GENICheterozygous139415099
14104334137104334137TAC26GENICheterozygous139415100
14104334389104334390TC26GENICheterozygous139614403
14104334391104334392GA24GENICheterozygous139614404
14104334395104334396TC24GENICheterozygous139614405
14104334397104334398TG24GENICheterozygous139614406
14104334402104334403GT25GENICheterozygous139614407
14104334409104334410TC25GENICheterozygous139614408
14104334413104334414TC27GENICheterozygous139614409
14104334416104334417GT27GENICheterozygous139614410
14104334421104334421CCAGA27GENICheterozygous139415101
14104334431104334433TG23GENICheterozygous139415104
14104334434104334434AA23GENICheterozygous139415105
14104334435104334436TC23GENICheterozygous139614411
14104334438104334438T22GENICheterozygous139415106
14104334464104334466TG29GENICheterozygous139415107
14104334468104334469AC29GENICheterozygous139614412
14104334470104334470GG27GENICheterozygous139415108
14104349897104349898G5GENIChomozygous141043840