chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122217875822178759AC26GENIChomozygous115280579
122217891322178914TA31GENIChomozygous115445684
122217896422178965GA28GENIChomozygous115445686
122217960722179608GA25GENIChomozygous115280583
122217961822179619TC24GENIChomozygous115280585
122217966222179663TC19GENIChomozygous115445688
122217969922179700TC29GENIChomozygous115445689
122218041122180412GA23GENIChomozygous115445691
122218089622180897TC33GENIChomozygous115280587
122218293522182936GA32GENIChomozygous115280591
122218297522182976TC26GENIChomozygous115280593
122218547222185473TC28GENIChomozygous115280595
122218612322186124TC28GENIChomozygous115280597
122218699022186991GA34GENIChomozygous115445693
122218754922187550TC26GENIChomozygous115280599
122218760522187606GA30GENIChomozygous115280601
122218806322188064TC13GENIChomozygous115280603
122218813022188131TC11GENIChomozygous115280605
122218962422189625GT40GENIChomozygous115280607
122219087222190873AT36GENIChomozygous115280609
122219105122191052TA27GENIChomozygous115280611
122219156422191565TA30GENIChomozygous115280613
122219161222191613CT21GENIChomozygous115366495
122219172222191723GC19GENIChomozygous115280615
122219203922192040GA16GENIChomozygous115280617
122219233622192337TC21GENIChomozygous115280619
122219301522193016CT21GENIChomozygous115280623
122219318222193183TC34GENIChomozygous115280625
122219391922193920GA19GENIChomozygous115280627