chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96950710469507105G12GENIChomozygous128721564
96950712969507130G13GENIChomozygous128721565
96951282369512827AAAA18GENIChomozygous128721566
96951282969512830AT18GENIChomozygous117584020
96951282969512829C18GENIChomozygous128721567
96951349069513491C21GENIChomozygous128721568
96951349569513496A21GENIChomozygous128721569
96951356069513560G18GENIChomozygous128721570
96951367369513673T23GENIChomozygous128721571
96951377269513772T16GENIChomozygous128721572
96951381869513819A18GENIChomozygous128721573
96951391269513912G28GENIChomozygous128721574
96951393269513933A27GENIChomozygous128721575
96951394869513949A26GENIChomozygous128721576
96951395169513952G26GENIChomozygous128721577
96954787769547878TC15GENICpossibly homozygous117372807
96954783569547836AG23GENICheterozygous117372805
96959131469591315A14GENICheterozygous131069661