chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15390411353904113T13GENICheterozygous141084187
15403329454033295CT22GENICheterozygous403697012
15403329754033298CG21GENICheterozygous403697013
15403320954033210AT22GENICheterozygous403916857
15403326154033262CA21GENICheterozygous403916858
15403369254033693TC34GENICheterozygous135546841
15403381454033815GC104GENICheterozygous135546843
15403366654033667TC21GENICheterozygous140853219
15403367454033675CG23GENICheterozygous140853220
15403381354033814TC105GENICheterozygous135546842
15403381854033819TG100GENICpossibly homozygous135546845
15403383554033836GA97GENICheterozygous135546846
15403383554033836G97GENICheterozygous402947372
15403383954033840AG92GENICheterozygous135546847
15403384054033841AT92GENICheterozygous135546848
15403386654033867CT81GENICheterozygous135546849
15403390654033907CA52GENICheterozygous402947373
15403391154033912TA48GENICheterozygous402947374
15403394954033950AT23GENICheterozygous402947375
15403396254033963CG18GENICheterozygous402947376