chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122465483724654838GT10GENICpossibly homozygous50135529
122465484824654849GA11GENIChomozygous50135531
122465519324655194CT13GENIChomozygous50135533
122465529324655294GA18GENIChomozygous50135535
122465547224655473GA10GENICpossibly homozygous50135538
122465629424656295AG8GENIChomozygous50135540
122465687124656872CCA4GENICheterozygous50135544
122465720424657205AG6GENICheterozygous50135546
122465722024657221CCATGAAAGGCATCAAAAAAA2GENIChomozygous50508216
122465726924657271GG--3GENICheterozygous50135550
122465727024657271G-3GENICheterozygous50293526
122465727524657276GT3GENICheterozygous50508218
122465752324657524GA11GENICheterozygous50135552
122465761324657614GA8GENICpossibly homozygous50135554
122465770524657706GA8GENICpossibly homozygous50135556
122465776724657768CT12GENIChomozygous50135558
122465937024659371TC12GENIChomozygous50418495
122466306224663086GAGAGAGAGAGAGAGAAAGAGAGA------------------------1GENIChomozygous50508220
122466313424663135GA5GENICheterozygous50135588
122466351224663513CT8GENIChomozygous50135590
122466353324663535TT--4GENIChomozygous50135592