chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13103396387103396388GA28GENIChomozygous49872385
13103396689103396690AG30GENICpossibly homozygous49872386
13103396962103396963A-20GENIChomozygous49872387
13103398351103398352AG9GENIChomozygous49872388
13103399855103399856GGGTGTGTGTGTGTGTGTGT12GENICheterozygous50838291
13103399857103399858TTGG4GENICheterozygous49872389
13103400011103400012AG22GENICpossibly homozygous49872390
13103400922103400923TC21GENICpossibly homozygous49872391
13103401882103401883AG12GENIChomozygous49872392
13103403084103403085TC24GENIChomozygous49872401
13103403525103403526TG26GENIChomozygous49872402
13103404007103404008AG12GENIChomozygous49872403
13103404191103404192TA1GENIChomozygous49872404
13103404201103404202AG9GENIChomozygous49872405
13103404532103404533CT21GENICpossibly homozygous49872406
13103404933103404934CCACACACACACACACACACACACAT6GENICheterozygous50597261
13103405017103405018GT23GENICpossibly homozygous49872407
13103405090103405091TTAG6GENIChomozygous49872408
13103405468103405469GA9GENIChomozygous49872409
13103405818103405819TA15GENIChomozygous49872412
13103406234103406235TC14GENIChomozygous49872413
13103406524103406525TC19GENIChomozygous49872414