chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106581154765811548C29GENIChomozygous128826014
106581158465811585AC30GENIChomozygous116619493
106581191265811913AG36GENIChomozygous116619495
106581236365812364GA25GENIChomozygous116793381
106581246365812464AG27GENIChomozygous116619497
106581312865813129CG35GENIChomozygous116619499
106581381465813814AGGGCCTTGCGCTTGCT14GENIChomozygous128826015
106581387565813876CT21GENIChomozygous116793383
106581449665814497AG20GENIChomozygous116793385
106581464465814645AG36GENIChomozygous116619503
106581569265815694TT24GENIChomozygous128826016
106581715265817152ATC33GENIChomozygous128826017
106581757965817580CG30GENIChomozygous116619507
106581803365818034AG31GENIChomozygous116619511
106581943865819439CT38GENIChomozygous116619517
106582000965820010AG33GENIChomozygous116793387
106581599565815996AG18GENIChomozygous117998758
106581457665814583CAATCCA31GENIChomozygous131095969
106581539965815400AC17GENICpossibly homozygous116978719
106581540765815408AC17GENICpossibly homozygous116978721