chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108774652287746523CT104GENICheterozygous51532718
108774654587746546GT129GENICheterozygous51532719
108774666987746670GA58GENICheterozygous51532720
108774695687746957GT49GENICheterozygous51532732
108774709987747100CT67GENICheterozygous53568810
108774710087747101AG67GENICheterozygous53568811
108774710187747102GA67GENICheterozygous53568812
108774710287747103AG68GENICheterozygous53568813
108774719687747197CA83GENICheterozygous51532734
108774886487748865AG97GENICheterozygous51532739
108774900087749001TC84GENICheterozygous51532741
108774906287749063GA46GENICheterozygous51728349
108774906587749066CT38GENICheterozygous51532742
108774910187749102GA36GENICheterozygous51532743
108774912587749126TG35GENICheterozygous51532744
108774917587749176GA43GENICheterozygous51532746