chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6115096625115096626AG56GENICheterozygous56298103
6115096914115096915CT47GENICheterozygous56298104
6115097145115097146GGC50GENICheterozygous56298105
6115097198115097199GA53GENICheterozygous54657203
6115097225115097226GGCAGATGCA56GENICheterozygous54657205
6115098265115098266CCA45GENICheterozygous54657207
6115098266115098267TG40GENICheterozygous55427649
6115098409115098410AC25GENICheterozygous56107173
6115110827115110828AC28GENICheterozygous55049811
6115113887115113888GC18GENICheterozygous55049815
6115113941115113942CG29GENICheterozygous55049816
6115113999115114000CT28GENICheterozygous56298130
6115127576115127577GT5GENICheterozygous55049872
6115130705115130706CT23GENICheterozygous55049884
6115132569115132570TA7GENICheterozygous55049889
6115135041115135042CT8GENICheterozygous55049909
6115135433115135434AG24GENICheterozygous55049910
6115137749115137750AT17GENICheterozygous55049933
6115140780115140781TC13GENICheterozygous55049948
6115142928115142929CT68GENICheterozygous55049961
6115145110115145111TC6GENICheterozygous55049967
6115145264115145265GA24GENICheterozygous56298131
6115150106115150107GA11GENICheterozygous56298132
6115150280115150281GA9GENICheterozygous56298133
6115150281115150282GA9GENICheterozygous56298134