chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140222794140222795TC29GENICheterozygous69178729
7140222833140222834AG40GENICpossibly homozygous69178731
7140223570140223571AG2GENIChomozygous69178733
7140223615140223616CT10GENIChomozygous69388196
7140223642140223643CT16GENICheterozygous69178734
7140223648140223649TA15GENICheterozygous69178735
7140224339140224340CT39GENIChomozygous69178736
7140224801140224802TC39GENIChomozygous69178737
7140224940140224941TA30GENIChomozygous69178739
7140225035140225036GA43GENIChomozygous69178740
7140225370140225371GC20GENICpossibly homozygous69388197
7140225383140225384CG18GENIChomozygous69178742
7140225588140225589TC53GENIChomozygous69178743
7140227280140227281GC38GENIChomozygous69178745