chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104641216446412165CT20GENIChomozygous142240074
104641789946417900AG20GENICheterozygous154636904
104642186346421864GA26GENIChomozygous138784854
104641668246416683GA23GENIChomozygous138784851
104641819846418199AG22GENIChomozygous138784852
104641927346419274TC24GENIChomozygous138784853
104641789946417900A20GENICheterozygous403938325
104642575246425753AG23GENIChomozygous142240075
104642591146425912CT23GENIChomozygous138784856
104642671446426715AT25GENIChomozygous138784857
104642768946427690AT23GENIChomozygous138784860
104643029846430299TC24GENIChomozygous138784861
104643336946433370CA28GENIChomozygous138784865
104643393046433931AG15GENIChomozygous138784866
104643749146437492GA23GENIChomozygous142240076
104642516546425166T29GENIChomozygous138682341
104641789846417902AAAC20GENICheterozygous149496861
104642516746425196TCTCTCTCTCTCTCTCTCTCTCTCTCTCT29GENIChomozygous138682342
104642990746429907A17GENIChomozygous138682344
104643598746435988A14GENIChomozygous138682346
104644280646442807TC26GENIChomozygous138784868
104644416146444162TG23GENIChomozygous138784869
104643368846433688T21GENIChomozygous142201726