chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115007643350076434C-2GENICheterozygous50880695
115007678550076786T-14GENIChomozygous50774753
115008196950081970A-7GENICheterozygous51183802
115008835250088353AAG12GENICheterozygous51294767
115009086950090872GGG---6GENICheterozygous51183804
115010844050108441CCTTT33GENICheterozygous50774759
115010849150108492T-37GENICheterozygous50774761
115010850650108507TTTA42GENICheterozygous50774762
115010853250108533TTTATAA45GENICheterozygous50774763
115010864950108650TTA26GENICheterozygous50774767
115010913450109137ATA---36GENICheterozygous50774773
115010944550109446G-28GENICheterozygous50774782
115010953450109535CCA20GENICheterozygous51161782
115010960350109604T-19GENICheterozygous51183808
115011374650113747TG14GENIChomozygous50774784
115011374750113748TG13GENIChomozygous50774785
115011384350113844CG23GENIChomozygous50774786
115011385850113859GC22GENIChomozygous50774787
115011386050113861AG22GENIChomozygous50774788
115011759550117596G-3GENIChomozygous51195976
115012127550121276C-18GENIChomozygous50774791
115012891550128916GC21GENIChomozygous50774792
115012892250128923TC20GENIChomozygous50774793
115012893250128933AG17GENIChomozygous50774794
115012893350128934CT17GENIChomozygous50774795
115012894550128946TC17GENIChomozygous50774796
115012897750128978CCA12GENIChomozygous50774797
115012903350129034A-2GENIChomozygous50774798
115012903750129038TTC2GENIChomozygous50774799
115012922450129225G-2GENIChomozygous50774803
115016129850161299CCTTT3GENICheterozygous51183816
115017082250170826AAGG----12GENIChomozygous51469201
115018406650184067T-6GENICheterozygous51195983
115018603850186039AT42GENICpossibly homozygous50774818
115018786850187869GT25GENIChomozygous50774820
115018836650188367T-30GENIChomozygous50774822
115019483550194836CG12GENIChomozygous50774823
115019634850196350AC--9GENICheterozygous51213602
115019890750198908CCA2GENICheterozygous51183818