chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3134684987134684990TTT---3GENIChomozygous57689004
3134684990134684991TA3GENIChomozygous58624925
3134685303134685304AG21GENIChomozygous57689006
3134685844134685845TA20GENIChomozygous58201565
3134685885134685886AG12GENIChomozygous59704416
3134686230134686231AG19GENIChomozygous57689009
3134686614134686615CT18GENIChomozygous57689011
3134686904134686905CCTTT2GENICheterozygous58624926
3134688251134688252GA19GENIChomozygous60027501
3134687794134687795CCT15GENIChomozygous60027497
3134688125134688126TTC12GENICpossibly homozygous60027499
3134689145134689146TTTTTG5GENIChomozygous57689016
3134689185134689186T-12GENIChomozygous58395372
3134692735134692736TC12GENIChomozygous57689019
3134693925134693926TC14GENIChomozygous60027503
3134691911134691912CCACATACAT5GENIChomozygous59048283