chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122375302723753028TC16GENIChomozygous115285700
122375389223753893CA14GENIChomozygous115368610
122375540223755403TC18GENIChomozygous115285704
122375555623755557CT10GENIChomozygous118341326
122375665623756657TC4GENIChomozygous115285710
122375829623758297AG28GENIChomozygous115285712
122375842423758425CT15GENIChomozygous115368614
122375863123758632TC28GENIChomozygous115285716
122375907923759080CT14GENIChomozygous115368616
122375931723759318AG15GENIChomozygous115285718
122375967223759673GA27GENIChomozygous115368618
122376091623760917GC4GENIChomozygous115285726
122376143323761434GA9GENIChomozygous115368620
122376253523762536AG15GENIChomozygous115285730
122376487223764873AG14GENIChomozygous115368626
122376534523765346AG25GENIChomozygous115285738
122376859923768600GA19GENIChomozygous115368630
122376871723768718CT11GENIChomozygous115368632
122376902023769021AG6GENICheterozygous118301140
122376932623769327TC25GENIChomozygous115285760
122375560823755609CT5GENIChomozygous115703393
122376758123767582CA5GENICheterozygous126221092