chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2048923234892324GA107GENICheterozygous783121268
2048923344892335GC116GENICheterozygous783121269
2048923414892342CT121GENICheterozygous783121270
2048923934892394AG123GENICheterozygous783121271
2048923964892397GC119GENICheterozygous783121272
2048924974892498GT83GENICheterozygous783121273
2048928124892813GT63GENICheterozygous783121274
2048928784892879TC103GENICheterozygous783121275
2048928894892890AG118GENICheterozygous783121276
2048928974892898TA122GENICheterozygous783121277
2048929154892916CT121GENICheterozygous783121278
2048929304892931GC123GENICheterozygous783121279
2048929524892953TC169GENICheterozygous783121280
2048929624892963AT174GENICheterozygous783121281
2048929664892967TC141GENICheterozygous783121282
2048929684892969AG179GENICheterozygous783121283
2048929964892997AG250GENICheterozygous783121284
2048929974892998AG193GENICheterozygous783121285
2048930074893008AG250GENICheterozygous783121286
2048930584893059TC249GENICheterozygous783121287
2048930884893089GA248GENICheterozygous783121288
2048931104893111CT248GENICheterozygous783121289
2048931664893167AG248GENICheterozygous783121290