chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140222794140222795TC39GENICheterozygous69178729
7140222833140222834AG33GENIChomozygous69178731
7140223570140223571AG14GENIChomozygous69178733
7140223615140223616CT29GENIChomozygous69388196
7140223642140223643CT34GENICpossibly homozygous69178734
7140223648140223649TA36GENICpossibly homozygous69178735
7140224339140224340CT38GENIChomozygous69178736
7140224801140224802TC25GENIChomozygous69178737
7140224940140224941TA38GENIChomozygous69178739
7140225035140225036GA39GENIChomozygous69178740
7140225383140225384CG21GENIChomozygous69178742
7140225588140225589TC54GENIChomozygous69178743
7140225994140225995CA63GENICheterozygous69178744
7140227280140227281GC14GENIChomozygous69178745