chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123593486635934867GT19GENICpossibly homozygous139137119
123594042335940424CA27GENIChomozygous139137120
123594435935944360AC24GENIChomozygous139137121
123594444735944448AG25GENIChomozygous139137122
123594581335945814GA24GENIChomozygous139137123
123594895035948951TG22GENIChomozygous139137124
123594675435946768TGTGTGTGTGTGTT13GENICheterozygous139054026
123594053135940532G15GENIChomozygous139054025