chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3152400051152400052AG56GENIChomozygous148870523
3152400250152400251AC44GENIChomozygous148870524
3152400376152400377CT47GENIChomozygous148870525
3152400896152400896T48GENICpossibly homozygous148861878
3152402822152402823CT52GENIChomozygous148870526
3152404126152404127AG51GENIChomozygous148870527
3152404137152404138AG48GENIChomozygous148870528
3152404271152404272TC40GENIChomozygous136840836
3152405709152405710TC49GENIChomozygous136840838
3152405973152405974GA46GENIChomozygous148870529
3152407994152407995TC53GENIChomozygous136840839
3152408215152408216TC53GENIChomozygous136840841
3152410541152410542TC51GENIChomozygous136840844
3152413093152413094AT52GENIChomozygous136840847
3152401296152401297C43GENIChomozygous136595976
3152409819152409823GAAG56GENIChomozygous136595979
3152412577152412577C48GENIChomozygous136595980
3152412900152412901A49GENIChomozygous136595981
3152414489152414490GA27GENIChomozygous148870530
3152414788152414789TC53GENIChomozygous136840848
3152415411152415412GA45GENIChomozygous148870531
3152416309152416310TA29GENIChomozygous136840849
3152417778152417779CT41GENIChomozygous136840851
3152417833152417834GA55GENIChomozygous136840852
3152418902152418903CT54GENICpossibly homozygous136840854
3152420627152420633ACACAT21GENICheterozygous148861879
3152421870152421874CTCA50GENIChomozygous148861880
3152422830152422831TA66GENIChomozygous136840860