chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101542977101542978CT15GENIChomozygous783564066
1101543926101543927AG16GENIChomozygous783564067
1101544542101544543AG18GENIChomozygous783564068
1101544986101544987TC21GENIChomozygous783564069
1101545354101545355TC17GENIChomozygous783564070
1101545661101545662AG21GENIChomozygous783564071
1101545796101545797CT21GENIChomozygous783564072
1101545823101545824AG27GENIChomozygous783564073
1101546322101546323GC21GENIChomozygous783564074
1101546435101546436TG14GENICheterozygous783564075
1101547798101547799AG28GENIChomozygous783564076
1101547896101547897TC17GENIChomozygous783564077