chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140222794140222795TC51GENICheterozygous69178729
7140222806140222807TC58GENICheterozygous69178730
7140222833140222834AG47GENIChomozygous69178731
7140223570140223571AG7GENIChomozygous69178733
7140223615140223616CT14GENIChomozygous69388196
7140223642140223643CT46GENICheterozygous69178734
7140223648140223649TA48GENICheterozygous69178735
7140224339140224340CT41GENIChomozygous69178736
7140224801140224802TC34GENIChomozygous69178737
7140224940140224941TA30GENIChomozygous69178739
7140225035140225036GA40GENIChomozygous69178740
7140225370140225371GC30GENICpossibly homozygous69388197
7140225383140225384CG29GENIChomozygous69178742
7140225588140225589TC81GENIChomozygous69178743
7140227280140227281GC33GENIChomozygous69178745