chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138054730180547302CA36GENIChomozygous114405868
138056142580561426AT30GENIChomozygous114405912
138057218280572183GA34GENIChomozygous114566851
138057280880572809CT31GENIChomozygous114405936
138058257080582571CT22GENICpossibly homozygous114566852
138058641480586415GA24GENIChomozygous114566853
138058771480587715GT31GENIChomozygous114566855
138058791180587912AG33GENIChomozygous114405958
138058926780589268GA26GENIChomozygous114405960
138059042680590427AT24GENIChomozygous114405962
138059311680593117AG35GENIChomozygous114405964
138059465880594659AT29GENIChomozygous114405966
138059613580596136AG36GENIChomozygous114405968
138059851680598517TC29GENIChomozygous114405970
138059852980598530CT28GENIChomozygous114405972
138059883280598833AG19GENIChomozygous114405974
138059903580599036GA26GENIChomozygous114405976
138060220980602210CT30GENIChomozygous114405980
138060368880603689TC28GENIChomozygous114566856
138060621380606214CA21GENIChomozygous114566857
138060671680606717CT39GENIChomozygous114405992
138060976880609769TC27GENIChomozygous114405998
138061100280611003TC26GENIChomozygous114566858
138061153280611533CT18GENIChomozygous114566859
138058981380589814CG9GENIChomozygous114644377
138059943980599440CT22GENIChomozygous114644379