chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140222794140222795TC23GENICheterozygous69178729
7140222806140222807TC23GENICheterozygous69178730
7140222833140222834AG30GENIChomozygous69178731
7140223570140223571AG13GENIChomozygous69178733
7140223615140223616CT20GENIChomozygous69388196
7140223642140223643CT22GENICpossibly homozygous69178734
7140223648140223649TA24GENICpossibly homozygous69178735
7140224339140224340CT15GENIChomozygous69178736
7140224801140224802TC17GENIChomozygous69178737
7140224940140224941TA20GENICpossibly homozygous69178739
7140225035140225036GA21GENIChomozygous69178740
7140225370140225371GC13GENICheterozygous69388197
7140225383140225384CG10GENIChomozygous69178742
7140225588140225589TC40GENIChomozygous69178743
7140225994140225995CA34GENICheterozygous69178744
7140227280140227281GC21GENICpossibly homozygous69178745