chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122465483724654838GT29GENIChomozygous50135529
122465484824654849GA24GENIChomozygous50135531
122465519324655194CT35GENIChomozygous50135533
122465529324655294GA43GENIChomozygous50135535
122465547224655473GA44GENIChomozygous50135538
122465629424656295AG28GENIChomozygous50135540
122465686324656864TTC25GENIChomozygous50135542
122465687124656872CCA27GENIChomozygous50135544
122465720424657205AG14GENIChomozygous50135546
122465721624657218TC--12GENICheterozygous50135548
122465726924657271GG--13GENIChomozygous50135550
122465752324657524GA28GENIChomozygous50135552
122465761324657614GA24GENICpossibly homozygous50135554
122465770524657706GA24GENIChomozygous50135556
122465776724657768CT19GENIChomozygous50135558
122465937024659371TC26GENIChomozygous50418495
122466313424663135GA18GENICpossibly homozygous50135588
122466351224663513CT34GENIChomozygous50135590
122466353324663535TT--36GENIChomozygous50135592
122466354024663541TTG39GENIChomozygous50135596