chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109075401109075402TA20GENIChomozygous71675881
6109087205109087206CA23GENIChomozygous71675883
6109110538109110539AC14GENIChomozygous70528456
6109110663109110664TC7GENIChomozygous70528468
6109110683109110684AC6GENIChomozygous70528477
6109110684109110685GT6GENIChomozygous70528481
6109110783109110784TA1GENIChomozygous70528498
6109110785109110786TA1GENIChomozygous70528502
6109111777109111778GC18GENIChomozygous70528506
6109123849109123850GT15INTERGENIChomozygous70528514
6109132927109132928CT18GENIChomozygous70528551
6109133425109133426TC32GENIChomozygous70528558
6109133508109133509TA23GENIChomozygous71675885
6109141644109141645CT26INTERGENIChomozygous71675887
6109148401109148402GA22INTERGENIChomozygous71675889
6109150691109150692AG26INTERGENIChomozygous71675891
6109151376109151377AG23INTERGENIChomozygous70528665
6109152968109152969TC26INTERGENIChomozygous70528669
6109154007109154008GA15INTERGENIChomozygous71675893
6109154773109154774CT16INTERGENIChomozygous70528673
6109165879109165880GT23GENICpossibly homozygous70528707
6109167450109167451TC9GENICpossibly homozygous70528719
6109176348109176349GA21GENIChomozygous71675895
6109179687109179688AG23GENIChomozygous70528755