chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4129522023129522024TC40GENIChomozygous113241516
4129522048129522049GT43GENIChomozygous113159928
4129522512129522513CT54GENIChomozygous113241517
4129531977129531978GA41GENIChomozygous113241519
4129532155129532156AG65GENIChomozygous113241520
4129534149129534150AG70GENIChomozygous113159938
4129534601129534602CT49GENIChomozygous113241521
4129535985129535994TCCTGCTCC44GENIChomozygous131641863
4129538377129538377TAT57GENIChomozygous131641865
4129538584129538585GA59GENIChomozygous113159940
4129539099129539100G40GENIChomozygous131641866
4129540855129540856TC51GENIChomozygous113159942
4129542277129542278GA70GENIChomozygous113241522
4129544157129544158TG66GENIChomozygous113241523
4129527722129527722A51GENICpossibly homozygous132967016
4129545585129545589GATG58GENIChomozygous132967017