chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140222794140222795TC35GENICheterozygous69178729
7140222833140222834AG37GENIChomozygous69178731
7140223570140223571AG14GENIChomozygous69178733
7140223615140223616CT23GENIChomozygous69388196
7140223642140223643CT26GENICpossibly homozygous69178734
7140223648140223649TA29GENICpossibly homozygous69178735
7140224339140224340CT30GENIChomozygous69178736
7140224801140224802TC27GENIChomozygous69178737
7140224940140224941TA23GENIChomozygous69178739
7140225035140225036GA19GENIChomozygous69178740
7140225370140225371GC24GENICpossibly homozygous69388197
7140225383140225384CG25GENIChomozygous69178742
7140225588140225589TC50GENIChomozygous69178743
7140225994140225995CA51GENICheterozygous69178744
7140227280140227281GC23GENIChomozygous69178745