chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109074113109074114TC18GENIChomozygous70528418
6109079045109079046AC19GENICheterozygous71920771
6109087205109087206CA30GENIChomozygous71675883
6109110538109110539AC36GENIChomozygous70528456
6109110607109110608CA19GENICpossibly homozygous70528460
6109110658109110659TA9GENIChomozygous70528464
6109110663109110664TC8GENIChomozygous70528468
6109110677109110678CA5GENIChomozygous70528472
6109110683109110684AC4GENIChomozygous70528477
6109110684109110685GT4GENIChomozygous70528481
6109110695109110696GT3GENIChomozygous70528486
6109111777109111778GC44GENIChomozygous70528506
6109116594109116595GA27GENICheterozygous73224909
6109123849109123850GT26INTERGENIChomozygous70528514
6109132927109132928CT46GENIChomozygous70528551
6109133425109133426TC28GENIChomozygous70528558
6109133508109133509TA37GENIChomozygous71675885
6109141644109141645CT37INTERGENIChomozygous71675887
6109143992109143993AG30INTERGENICheterozygous70528623
6109143996109143997GA32INTERGENICheterozygous70528627
6109148401109148402GA50INTERGENIChomozygous71675889
6109150691109150692AG24INTERGENIChomozygous71675891
6109151376109151377AG27INTERGENIChomozygous70528665
6109152968109152969TC27INTERGENIChomozygous70528669
6109154007109154008GA44INTERGENIChomozygous71675893
6109154773109154774CT31INTERGENIChomozygous70528673
6109160448109160449TA28GENIChomozygous70528691
6109165879109165880GT22GENICpossibly homozygous70528707
6109167399109167400AG18GENICheterozygous70528711
6109167426109167427TA9GENIChomozygous70528715
6109167450109167451TC17GENIChomozygous70528719
6109167460109167461GA18GENIChomozygous70528723
6109167483109167484GC23GENIChomozygous70528727
6109176348109176349GA41GENIChomozygous71675895
6109179687109179688AG39GENIChomozygous70528755