chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104858755648587557CT50GENICpossibly homozygous116879995
104858912448589124GAA54GENIChomozygous131092888
104859015048590151AG52GENIChomozygous116879997
104859065748590658A56GENIChomozygous131092889
104859127648591277TC51GENIChomozygous117410573
104859219348592194TC63GENIChomozygous116879999
104859249848592499TC50GENIChomozygous116880001
104859278348592784CT46GENIChomozygous116880003
104859286648592867TC48GENIChomozygous116880005
104859359148593592CT71GENIChomozygous116880007
104859370848593709TG54GENIChomozygous116880009
104859408948594090A37GENIChomozygous131092890
104859411148594111GG36GENIChomozygous131092891
104859413948594140CT31GENIChomozygous117218378
104859809248598093GA49GENIChomozygous116880011
104859866548598666CA66GENIChomozygous116880013
104859867448598675CT67GENIChomozygous116880015
104859139948591400A52GENIChomozygous129968926