chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124041843040418431GGT36INTERGENIChomozygous50203518
124041854940418550TC25INTERGENIChomozygous50203521
124041857040418571GT20INTERGENIChomozygous50203522
124041859240418593GGT13INTERGENIChomozygous50203523
124041860940418610C-10INTERGENIChomozygous50203524
124041865640418657G-13INTERGENIChomozygous50203525
124041933640419337CCAGAATA4INTERGENIChomozygous50203528
124041938540419386AT3INTERGENIChomozygous50203529
124042385840423859CCT2INTERGENIChomozygous50203535
124042832040428321A-20INTERGENICheterozygous50203537
124042851440428515T-14INTERGENICheterozygous50452208
124043047640430477T-23INTERGENICheterozygous50203542
124043049140430492TC29INTERGENICpossibly homozygous50452209
124043143440431436TG--16INTERGENICheterozygous50203545
124043307640433077GGT15INTERGENIChomozygous50203547
124043332340433324AG48INTERGENIChomozygous50452210
124043342240433423CT34INTERGENIChomozygous50452211
124043355940433560AG14INTERGENIChomozygous50203549
124045638040456381AG31GENICheterozygous50203570
124045638440456385CCA21GENICheterozygous50203572
124045659440456595TG38GENICheterozygous50381646