chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106145774361457744AG22GENICheterozygous52306870
106146007861460079CCAG19GENICheterozygous51470873
106146305961463061AC--18GENICpossibly homozygous51670505
106146309761463098AACAC32GENICheterozygous51470874
106146621961466220GGT16GENIChomozygous51470876
106147268861472689AT27GENIChomozygous52249255
106148252961482530CT3GENIChomozygous51470883
106149042061490421TTTC5GENIChomozygous51670550
106149045061490451TC16GENICheterozygous51899808
106153351361533514TTA4GENIChomozygous51470889
106153353361533534TG5GENIChomozygous51470890
106153355761533558GC5GENIChomozygous51470891
106153356761533568GA5GENIChomozygous51470895
106153357061533571CT5GENIChomozygous51470896
106153358761533588CT2GENIChomozygous51470897
106154610861546109CCA17GENIChomozygous51470903
106154785261547853GGT6GENIChomozygous51670568
106155222461552225AG37GENIChomozygous51470905
106155684161556842CCTG27GENICpossibly homozygous51670584
106156533361565334GGA16GENIChomozygous51470911
106156570461565705AG25GENIChomozygous52249257
106156791661567917GT26GENIChomozygous51470913
106156870061568701TC9GENICheterozygous51470914
106157008561570086TC18GENIChomozygous52249259
106157373361573736CTT---7GENIChomozygous52249261
106157448861574491AAA---1GENIChomozygous51470916
106157732961577330T-14GENICheterozygous51470918
106157733461577335GGAT14GENICheterozygous51470919