chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13103396387103396388GA16GENICheterozygous49872385
13103398351103398352AG18GENICheterozygous49872388
13103400011103400012AG13GENICheterozygous49872390
13103400922103400923TC13GENICheterozygous49872391
13103401882103401883AG20GENICheterozygous49872392
13103402293103402294CT10GENICheterozygous49872393
13103402301103402302TC12GENICheterozygous49872394
13103403084103403085TC15GENICheterozygous49872401
13103403525103403526TG22GENICheterozygous49872402
13103404007103404008AG21GENICheterozygous49872403
13103404191103404192TA19GENICheterozygous49872404
13103404201103404202AG21GENICheterozygous49872405
13103404532103404533CT17GENICheterozygous49872406
13103405017103405018GT12GENICheterozygous49872407
13103405090103405091TTAG14GENIChomozygous49872408
13103405468103405469GA18GENICheterozygous49872409
13103405731103405741ATACACACAC----------17GENICheterozygous49872410
13103405750103405751CT15GENICheterozygous49872411
13103405818103405819TA21GENICheterozygous49872412
13103406234103406235TC19GENICheterozygous49872413
13103404933103404934CT7GENICheterozygous51282038
13103405748103405749CG14GENICheterozygous51282039
13103406524103406525TC14GENICheterozygous49872414