chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122217875822178759AC15GENIChomozygous115280579
122217960322179604CA25GENIChomozygous115280581
122217960722179608GA23GENIChomozygous115280583
122217961822179619TC20GENIChomozygous115280585
122218089622180897TC15GENIChomozygous115280587
122218202922182030GC26GENIChomozygous115280589
122218293522182936GA25GENIChomozygous115280591
122218297522182976TC23GENICpossibly homozygous115280593
122218547222185473TC20GENIChomozygous115280595
122218612322186124TC22GENIChomozygous115280597
122218754922187550TC21GENIChomozygous115280599
122218760522187606GA14GENIChomozygous115280601
122218806322188064TC21GENIChomozygous115280603
122218813022188131TC13GENIChomozygous115280605
122218899022188991TG17GENIChomozygous115366493
122218962422189625GT27GENIChomozygous115280607
122219161222191613CT17GENIChomozygous115366495
122219087222190873AT18GENIChomozygous115280609
122219105122191052TA26GENICpossibly homozygous115280611
122219156422191565TA19GENIChomozygous115280613
122219172222191723GC18GENIChomozygous115280615
122219203922192040GA18GENIChomozygous115280617
122219233622192337TC26GENIChomozygous115280619
122219293922192940CG17GENIChomozygous115280621
122219301522193016CT15GENIChomozygous115280623
122219318222193183TC19GENIChomozygous115280625
122219391922193920GA18GENIChomozygous115280627