chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124634452246344523TC15INTERGENICheterozygous50340058
124635072946350730GA29INTERGENICheterozygous50340112
124635187946351881AT--8INTERGENICheterozygous50340130
124636024946360250CT13GENICheterozygous50340179
124636816446368165AAT26GENICheterozygous50340251
124636828146368282GA11GENICheterozygous50340253
124636990546369906AG25GENICheterozygous50340270
124637290246372903AC5GENICheterozygous50340290
124638211446382115GT9GENICheterozygous50340326
124638820246388203AC37GENICheterozygous50340455
124638826946388270A-54GENICheterozygous50340457
124639634046396341CT34GENICheterozygous50340552
124639639946396400AAC12GENICheterozygous50340554
124641758346417584TC18GENICheterozygous50340677
124643409146434093CC--26GENICheterozygous50340755
124645119346451194GA49GENICheterozygous50340852
124645297346452974CT12GENICheterozygous50340876
124645297446452975TG12GENICheterozygous50340878
124645314746453148AG17GENICheterozygous50340880
124645749946457500AG15GENICheterozygous50341028
124645754646457547AG13GENICheterozygous50341030
124645756446457565GA14GENICheterozygous50341032
124645822346458224AG35GENICheterozygous50341052
124646425446464255TC17GENICheterozygous50341097
124648147746481478CG22GENICheterozygous50341198
124648151446481515GA21GENICheterozygous50341200