chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117277718117277719CT23GENIChomozygous594280794
7117278883117278887ATAG----10GENIChomozygous726048481
7117279665117279666TTA24GENICheterozygous726048483
7117279665117279666TTAA24GENICheterozygous726048484
7117280092117280093TG35GENIChomozygous593746932
7117280909117280910AACT44GENIChomozygous726048485
7117281031117281032GA30GENIChomozygous594280795
7117281397117281398GGA12GENIChomozygous726048486
7117281415117281416CT14GENIChomozygous593746933
7117281700117281703TTT---7GENICheterozygous726048487
7117281702117281703T-7GENICheterozygous726048488
7117281806117281807TC18GENIChomozygous593746934
7117281822117281823AG15GENIChomozygous593746935
7117281935117281936GA22GENIChomozygous593746936
7117281997117282009ACACACACACAC------------3GENIChomozygous726048490
7117282333117282334GA34GENIChomozygous593746937
7117282930117282931CT25GENIChomozygous594280796
7117283083117283084TC28GENIChomozygous594280797
7117283088117283089TA29GENIChomozygous593746938
7117283089117283090TA30GENIChomozygous593746939
7117283128117283129TC30GENIChomozygous593746940
7117283316117283317CG21GENIChomozygous593746941
7117284081117284082AG25GENIChomozygous593746942
7117284141117284142AG17GENIChomozygous593746943
7117284150117284151GA17GENIChomozygous594280798
7117284976117284977TC23GENIChomozygous593746944
7117285229117285230AG11GENIChomozygous593746945
7117286069117286070TC33GENIChomozygous593746946
7117286425117286426CT31GENIChomozygous594280799