chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154948597849485979GC14GENIChomozygous112504604
154948638949486390GA17GENIChomozygous112504606
154948648649486487CG23GENIChomozygous112504608
154948653349486534CA25GENIChomozygous112504610
154948695349486954TC27GENIChomozygous112504612
154948704649487047GA20GENIChomozygous112504614
154948750549487506CT18GENIChomozygous112504616
154948841949488420GA13GENIChomozygous112504618
154949177949491780CT16GENIChomozygous112504620
154949343249493433AC23GENIChomozygous112504622
154949397049493971GA18GENIChomozygous112504624
154949426049494261AT19GENIChomozygous112504626
154949526449495265AC24GENIChomozygous112504628
154949621949496220TC14GENIChomozygous112504630
154949630549496306GA16GENIChomozygous112504632
154949635749496358CT12GENIChomozygous112504634
154949661149496612AG11GENIChomozygous112504636
154949749549497496AG24GENIChomozygous112504638
154949766349497664GA21GENIChomozygous112504640
154949766549497666TC22GENIChomozygous112504642
154950198549501986TC5GENIChomozygous112504648
154950202249502023TG5GENIChomozygous112504650
154950300149503002TC16GENIChomozygous113228432
154950320149503202CT11GENIChomozygous112504652
154950439549504396CT20GENIChomozygous112504654
154950448249504483CT27GENIChomozygous112504656
154950579249505793GT16GENIChomozygous112504658
154950603449506035CT10GENIChomozygous112504660
154950902249509023CT13GENIChomozygous112504662
154951210649512107CT13GENIChomozygous112504665
154951272249512723CT15GENIChomozygous112504667
154951273949512740TC18GENIChomozygous112504669
154951468349514684CT9GENIChomozygous112504671
154951479949514800GA2GENIChomozygous113053778