chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109087205109087206CA17GENIChomozygous71675883
6109110538109110539AC15GENIChomozygous70528456
6109110663109110664TC12GENIChomozygous70528468
6109110683109110684AC9GENIChomozygous70528477
6109110684109110685GT9GENIChomozygous70528481
6109110783109110784TA6GENIChomozygous70528498
6109110785109110786TA6GENIChomozygous70528502
6109111777109111778GC31GENIChomozygous70528506
6109123849109123850GT13INTERGENIChomozygous70528514
6109132927109132928CT22GENIChomozygous70528551
6109133425109133426TC26GENIChomozygous70528558
6109133508109133509TA18GENIChomozygous71675885
6109141644109141645CT20INTERGENIChomozygous71675887
6109148401109148402GA13INTERGENIChomozygous71675889
6109150691109150692AG16INTERGENIChomozygous71675891
6109151376109151377AG19INTERGENIChomozygous70528665
6109152968109152969TC13INTERGENIChomozygous70528669
6109154007109154008GA16INTERGENIChomozygous71675893
6109154773109154774CT19INTERGENIChomozygous70528673
6109165879109165880GT25GENICpossibly homozygous70528707
6109167450109167451TC14GENIChomozygous70528719
6109176348109176349GA19GENIChomozygous71675895
6109179687109179688AG16GENIChomozygous70528755
6109130497109130498CA22INTERGENIChomozygous81566822