chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104641216446412165CT24GENIChomozygous142240074
104641668246416683GA13GENIChomozygous138784851
104641819846418199AG13GENIChomozygous138784852
104641927346419274TC19GENIChomozygous138784853
104642186346421864GA22GENICpossibly homozygous138784854
104642575246425753AG15GENIChomozygous142240075
104642591146425912CT19GENIChomozygous138784856
104642671446426715AT22GENIChomozygous138784857
104642768946427690AT21GENIChomozygous138784860
104642990746429907A17GENIChomozygous138682344
104642516546425166T17GENIChomozygous138682341
104642516746425196TCTCTCTCTCTCTCTCTCTCTCTCTCTCT17GENIChomozygous138682342
104643029846430299TC24GENIChomozygous138784861
104643336946433370CA16GENIChomozygous138784865
104643368846433688T28GENIChomozygous142201726
104643393046433931AG15GENIChomozygous138784866
104643598746435988A16GENIChomozygous138682346
104643749146437492GA22GENIChomozygous142240076
104643777046437771A19GENICheterozygous138682347
104644280646442807TC14GENIChomozygous138784868
104644416146444162TG19GENIChomozygous138784869