chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37262730872627309TC22GENICpossibly homozygous57447269
37262740072627401GA6GENIChomozygous57447271
37262891272628913CT8GENIChomozygous57447273
37262898172628982CCTTCTCT4GENIChomozygous57447275
37262904272629043CT7GENICheterozygous57447277
37262904372629044CT7GENICheterozygous57447279
37262949872629499TC9GENICpossibly homozygous57447281
37262967172629672AC14GENIChomozygous57447283
37263007872630079CCG18GENIChomozygous57447285
37263022672630227TC19GENIChomozygous57447287
37263054072630541GGA2GENIChomozygous57447289
37263190772631908TC17GENIChomozygous57447291