chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134760419347604194AG24GENIChomozygous881189825
134760429447604295TC17GENICpossibly homozygous881189826
134760462947604630AC26GENIChomozygous881189827
134760488847604889TC21GENIChomozygous881189828
134760615447606155AT27GENIChomozygous881189829
134760690147606902CT11GENICheterozygous881189830
134760690547606906GA9GENICheterozygous881189831
134760693447606935AG18GENIChomozygous881189832
134760745647607457AG16GENIChomozygous881189833
134760745747607458GA14GENIChomozygous881189834
134760753447607535GT9GENICheterozygous881189835
134760759147607592GC16GENIChomozygous881189836
134760761647607617GA19GENIChomozygous881189837
134760813247608133TG23GENIChomozygous881189838
134760828147608282AG23GENIChomozygous881189839
134760874247608743AG24GENIChomozygous881189840
134760911147609112TA11GENICheterozygous881189841
134761107347611074AG23GENIChomozygous881189842
134761115847611159CT13GENIChomozygous881189843
134761289947612900GA11GENIChomozygous881189844