chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140222794140222795TC19GENIChomozygous69178729
7140222806140222807TC23GENIChomozygous69178730
7140222833140222834AG26GENIChomozygous69178731
7140222851140222852TC28GENICheterozygous69178732
7140223570140223571AG10GENIChomozygous69178733
7140223642140223643CT18GENICpossibly homozygous69178734
7140223648140223649TA18GENICpossibly homozygous69178735
7140224339140224340CT26GENIChomozygous69178736
7140224801140224802TC24GENIChomozygous69178737
7140224857140224858GT16GENIChomozygous69178738
7140224940140224941TA23GENIChomozygous69178739
7140225035140225036GA20GENIChomozygous69178740
7140225383140225384CG31GENIChomozygous69178742
7140225588140225589TC23GENIChomozygous69178743
7140225994140225995CA29GENICheterozygous69178744
7140227280140227281GC30GENIChomozygous69178745