chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112069813112069814T-38GENIChomozygous58424405
3112070354112070355AT12GENICheterozygous58424406
3112070398112070402ATAG----7GENIChomozygous57991103
3112070401112070402GGAT7GENIChomozygous57991106
3112071140112071141CT25GENIChomozygous58424407
3112071652112071653TC25GENIChomozygous57991115
3112072557112072558TC10GENIChomozygous57991118
3112072945112072946CCAGGAGAAGTG7GENIChomozygous57991121
3112072948112072949CG5GENIChomozygous57991124
3112072950112072952CA--5GENIChomozygous57991127
3112074298112074299AG24GENIChomozygous57991133
3112075607112075608T-19GENIChomozygous58424408
3112076556112076557CT14GENICheterozygous58389273
3112076592112076593CT11GENIChomozygous58424409
3112077449112077450TTA21GENIChomozygous58424410
3112079435112079436CT47GENICheterozygous57991142
3112079902112079903GA34GENIChomozygous57991145
3112079951112079952CT30GENIChomozygous58424411
3112080169112080170TC22GENIChomozygous58424412
3112080290112080291CT37GENIChomozygous58424413
3112080620112080621CT15GENIChomozygous58424414
3112080993112080994AG33GENIChomozygous57991148
3112082224112082225AG37GENIChomozygous58424415
3112083412112083413TG15GENIChomozygous57991151
3112083477112083478AG22GENIChomozygous57991154
3112083581112083582AG27GENIChomozygous57603011
3112083766112083767AT33GENIChomozygous57991157