chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159392514159392514G21GENIChomozygous127947674
3159398041159398042CA16GENIChomozygous111789542
3159398044159398045CA17GENIChomozygous111789544
3159398049159398050GA17GENIChomozygous111789546
3159405161159405161CT29GENIChomozygous127947675
3159405289159405290TG23GENIChomozygous111789548
3159407342159407342A21GENIChomozygous127947677
3159407487159407490TCC14GENIChomozygous127947678
3159407573159407574C18GENIChomozygous127947679
3159407588159407589C19GENIChomozygous127947680
3159407628159407628G16GENIChomozygous127947681
3159407683159407684AC15GENIChomozygous111789550
3159407706159407707T8GENIChomozygous129892506
3159407735159407735G1GENIChomozygous127947682
3159407874159407875GT13GENIChomozygous111789554
3159407890159407890T14GENIChomozygous127947683
3159407907159407908G15GENIChomozygous127947684
3159407914159407916TT14GENIChomozygous127947685
3159407917159407918T14GENIChomozygous127947686
3159407923159407925TT15GENIChomozygous127947687
3159407939159407941TT15GENIChomozygous127947688
3159407943159407944T15GENIChomozygous127947689
3159407964159407965G16GENIChomozygous127947691
3159407905159407906TG14GENIChomozygous127994851
3159407933159407934TG15GENIChomozygous127994852
3159407709159407710TC8GENIChomozygous129899805
3159407950159407953TTG16GENIChomozygous127947690
3159407968159407968T16GENIChomozygous127947692
3159408037159408037T17GENIChomozygous127947693
3159408101159408103CC21GENIChomozygous127947694
3159408116159408117T20GENIChomozygous127947695
3159408142159408143GT18GENIChomozygous111789556