chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134197137134197138AT47GENIChomozygous114015925
5134197325134197326GC45GENIChomozygous114015926
5134197335134197336AC46GENIChomozygous114015927
5134199756134199757TG21GENICheterozygous114533253
5134201506134201507GA32GENICheterozygous114533311
5134201843134201844CT40GENICheterozygous114533321
5134201877134201878CG46GENICheterozygous114533323
5134201929134201930CA46GENICheterozygous114533325
5134204395134204396TC74GENICheterozygous114533379
5134205282134205283GA38GENICheterozygous114533389
5134206121134206122TA64GENICheterozygous118858428
5134206131134206132GA62GENICheterozygous118858429
5134206221134206222GA69GENICheterozygous118858430
5134206223134206224AG72GENICheterozygous118858431
5134206258134206259CT61GENICheterozygous114533401
5134206368134206369GA48GENICheterozygous114533403
5134206406134206407TG62GENICheterozygous114015962
5134206419134206420TC59GENICheterozygous114533405
5134206440134206441GT70GENICheterozygous114015963
5134206464134206465TA72GENICheterozygous114533407
5134206466134206467GT71GENICheterozygous114533409
5134206476134206477AG68GENICheterozygous114015964
5134206519134206520AG77GENICheterozygous114533411
5134206615134206616CT73GENICheterozygous114015965
5134206617134206618GT71GENICheterozygous114015966
5134206667134206668CT74GENICheterozygous114533413
5134206707134206708CT70GENICheterozygous114015967
5134206730134206731AT70GENICheterozygous114533415
5134206744134206745AG78GENICheterozygous114015968
5134206769134206770GA77GENICheterozygous114015969
5134206790134206791AG82GENICheterozygous114015970
5134206886134206887CT86GENICheterozygous114533417
5134206887134206888GA83GENICheterozygous114015971