chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1158232091158232092AG14GENIChomozygous61769187
1158232701158232717TATCTATCTATCTATC----------------15GENIChomozygous62168143
1158233043158233044AG27GENIChomozygous60910897
1158233975158233976AATTT10GENICheterozygous60910899
1158233975158233976AATT10GENICheterozygous62270347
1158236539158236540AAACAC4GENICheterozygous61769191
1158236539158236540AAACACACACACAC4GENICheterozygous62343399
1158236658158236659TC31GENIChomozygous60910903
1158236149158236150GA17GENIChomozygous60910901
1158236659158236660TC31GENIChomozygous60910904
1158237783158237784GA22GENIChomozygous61769193
1158238057158238058AG9GENIChomozygous61769195
1158238610158238611GT23GENIChomozygous61769197
1158238773158238774TC13GENIChomozygous60910908
1158241510158241511A-22GENIChomozygous61769199
1158241523158241524GA24GENIChomozygous61769201
1158242253158242254AG20GENIChomozygous60910918
1158242374158242375GT27GENIChomozygous60910919
1158242434158242435TC29GENIChomozygous61769203
1158243106158243107TC35GENIChomozygous60910922
1158244230158244231GC19GENIChomozygous60910931
1158246272158246273AAG32GENIChomozygous60910942
1158246484158246485AC35GENIChomozygous60910943
1158246548158246549GA28GENIChomozygous61769205
1158246678158246679AT28GENIChomozygous61769207
1158246765158246766GT28GENIChomozygous61769209
1158247753158247754GA35GENIChomozygous61769211
1158251032158251033CT20GENIChomozygous61769213
1158252368158252369CT9GENIChomozygous61769215
1158252789158252790T-17GENIChomozygous60910945
1158254661158254664AAA---7GENICheterozygous62270348
1158254662158254664AA--7GENICheterozygous62168147
1158254663158254664A-7GENICheterozygous62247052
1158255907158255908AAAT15GENICpossibly homozygous61769217
1158259672158259673CT32GENIChomozygous60910952
1158259831158259832GT14GENIChomozygous60910953
1158261721158261722AAT25GENIChomozygous60910955
1158262970158262971T-21GENIChomozygous61769219
1158246273158246274TA32GENIChomozygous62090122