chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105776227957762280AT54GENICheterozygous118039422
105777086957770870GT34GENICheterozygous118123676
105777095757770958AT122GENICheterozygous118123677
105777098257770983AG83GENICheterozygous118123678
105777100557771006TG63GENICheterozygous118039426
105777113357771134CG210GENICheterozygous118123679
105777336857773369CT110GENICheterozygous117995156
105778603557786036GT105GENICheterozygous118039458
105779261357792614GT81GENICheterozygous117995173
105779262257792623GT87GENICheterozygous117995174
105779263157792632GA100GENICheterozygous117995175
105779263557792636CT105GENICheterozygous118123680
105779268157792682AG163GENICheterozygous117995177
105779270957792710CT155GENICheterozygous117995178
105779275957792760GA105GENICheterozygous118103796
105781830457818305AG19GENICheterozygous118074969
105781837957818380CA29GENICpossibly homozygous117995188
105781838557818386CT26GENICpossibly homozygous117995189
105781840857818409TC26GENICheterozygous117995190
105781842257818423AC23GENICheterozygous117995191
105781842957818430AG23GENICheterozygous117995192
105781844057818441TC21GENICheterozygous117995193
105783320557833206AG60GENIChomozygous116604506