chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2242797992242797993AG26GENIChomozygous110344477
2242798125242798126GA48GENICheterozygous110344480
2242798146242798147GT37GENICpossibly homozygous110344482
2242798154242798155CT43GENICheterozygous110344484
2242798586242798587CA24GENIChomozygous110344486
2242798764242798765GT35GENIChomozygous110344488
2242800637242800638AG19GENIChomozygous110344494
2242802666242802667TG21GENIChomozygous110344500
2242803478242803479TC37GENIChomozygous110344502
2242805576242805577AG21GENIChomozygous110344504
2242806618242806619CT43GENIChomozygous110344506
2242818363242818364CA26GENIChomozygous111187472
2242800687242800688CT22GENIChomozygous111187466
2242801968242801969GC36GENIChomozygous111187468
2242804227242804228CT40GENIChomozygous111187470
2242821766242821767TA30GENIChomozygous111187474
2242822644242822645AG38GENIChomozygous110344510
2242825068242825069TG23GENIChomozygous110344516
2242825259242825260CT29GENIChomozygous110344518
2242825514242825515CT33GENICpossibly homozygous111187476
2242826620242826621AG26GENIChomozygous110344520
2242827224242827225CG22GENIChomozygous111187478
2242828278242828279AG23GENIChomozygous111187480
2242828316242828317CG17GENIChomozygous110344524