chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79158859091588591GA21GENIChomozygous54021304
79158873391588734TTAC10GENICheterozygous54021305
79158873391588734TTACACACACACAC10GENICheterozygous54021306
79158879091588791CT25GENIChomozygous54021307
79158885791588858T-26GENIChomozygous54021308
79158896891588972AAAG----10GENICpossibly homozygous54021309
79158897191588972G-13GENIChomozygous54021310
79158945991589460GA32GENIChomozygous54021311
79159086591590866CA21GENIChomozygous54021312
79159110591591106AG25GENIChomozygous54021313
79159160791591608TC30GENIChomozygous54021314
79159178791591788CT26GENIChomozygous54208187
79159190191591902TC24GENIChomozygous54021315
79159192591591926C-27GENIChomozygous54208188
79159192891591929T-27GENIChomozygous54021316
79159203491592035TC20GENIChomozygous54021317
79159220291592203TC39GENIChomozygous54208189
79159223991592240AC40GENIChomozygous54208190
79159228991592290AG33GENIChomozygous54208191
79159276891592769TA21GENICpossibly homozygous54021319