chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212584172212584173GA11GENICheterozygous132008174
1212584409212584410GA14GENICheterozygous127576806
1212584416212584417TC15GENICheterozygous127576807
1212584486212584487AC15GENICheterozygous127576808
1212584753212584754AT15GENICheterozygous131795812
1212584767212584768AG13GENICheterozygous127576809
1212585496212585497AG37GENICheterozygous127576815
1212585561212585562GC36GENICheterozygous121172308
1212585568212585569GA36GENICheterozygous121172309
1212585599212585600GA38GENICheterozygous109056321
1212585482212585483GC30GENICheterozygous109056318
1212585485212585486CA31GENICheterozygous109056319
1212585584212585585CT39GENICheterozygous109056320
1212585671212585672AG40GENICheterozygous127576816
1212587835212587836AG24GENICheterozygous121172311
1212587838212587839AC24GENICheterozygous127576824
1212587841212587842GA25GENICheterozygous127576825
1212587863212587864AG28GENICheterozygous109366855
1212588525212588527AA13GENICheterozygous127480428
1212588600212588601GA21GENICheterozygous127576826
1212588638212588638C20GENICheterozygous129844870
1212588863212588864TC25GENICheterozygous127576828
1212589089212589090GA17GENICheterozygous130852396
1212585612212585613AG38GENICheterozygous108526774
1212587956212587957CT36GENICheterozygous108526776
1212588829212588830GA28GENICheterozygous108526778
1212585695212585696G43GENICheterozygous131992040
1212599473212599474TC14GENIChomozygous108526780