chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123906090139060902T-7GENIChomozygous50542466
123906176239061763TTA1GENIChomozygous50600877
123906221339062217TCGT----14GENIChomozygous50196923
123906222439062225GA15GENIChomozygous50946021
123906223839062239TTTAG16GENIChomozygous50542470
123906224339062246TAC---18GENIChomozygous50542471
123906224739062248CG18GENIChomozygous50196925
123906227139062272TG19GENIChomozygous50196927
123906227639062277CA19GENIChomozygous50196929
123906227839062279TG18GENIChomozygous50196931
123906228539062289ACCC----20GENIChomozygous50542472
123906229039062291A-18GENIChomozygous50542473
123906229139062292AG18GENIChomozygous50542474
123906229339062294GGGTTGGC16GENIChomozygous50542475
123906229539062296CG15GENIChomozygous50542476
123906230439062305TA13GENIChomozygous50196935
123906231139062312CG13GENIChomozygous50196937
123906231339062314CG13GENIChomozygous50196939
123906231639062317CG13GENIChomozygous50196941
123906229839062299CG14GENIChomozygous50542477
123906230139062303TT--14GENIChomozygous50542478
123906267639062677A-12GENICpossibly homozygous50196943
123906268839062689CCAA7GENIChomozygous50196945
123906852239068523CCAAAAAAAAAA18GENIChomozygous50542484
123906902139069022TTA4GENICheterozygous50322894
123906902239069023A-4GENICheterozygous50322896
123906941439069415TC22GENICpossibly homozygous50196976
123907019539070196CCTTT13GENIChomozygous50542486
123907148739071488CA21GENICpossibly homozygous50946024
123907151239071513AG29GENICpossibly homozygous50196990
123907178539071786TC27GENIChomozygous50196992
123907270539072707AA--13GENIChomozygous50542488
123907888439078888TGTC----19GENICpossibly homozygous50946027
123908075539080756GT18GENIChomozygous50197020
123908086139080863GG--7GENICheterozygous50558883
123908267639082677T-7GENICheterozygous50599032
123907459739074598AAGAGGG10GENIChomozygous50640176