chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58250390982503910TA23GENIChomozygous648554228
58250400682504007A-29GENIChomozygous756208393
58250413182504132CT28GENIChomozygous648554229
58250456482504565AAG16GENIChomozygous756208394
58250464182504642GGA13GENIChomozygous756208395
58250526082505261TC21GENIChomozygous648554230
58250527982505280CCT12GENICheterozygous756208396
58250527982505280CCTT12GENICheterozygous756208397
58250572982505730TTCC2GENICheterozygous756208398
58250602582506026CT19GENIChomozygous648554231
58250644182506442A-11GENICpossibly homozygous756208399
58250663782506638TC25GENIChomozygous648554232
58250776582507766TC14GENIChomozygous648554233
58250807382508074AC9GENIChomozygous648554234
58250807882508084CTCTCT------7GENIChomozygous756208401
58250860582508607TC--23GENIChomozygous756208402
58250862382508624CCTGTG26GENIChomozygous756208403
58250875182508767GTGTGTGTGTGTGTGT----------------18GENIChomozygous756208404
58250895182508952TTTG22GENIChomozygous756208408
58250913982509140T-21GENIChomozygous756208410
58250924782509248TC23GENIChomozygous648554235
58250939982509400CT18GENIChomozygous648554236
58250942982509430GT18GENIChomozygous648554237
58250947382509474CA19GENIChomozygous648554238
58250993882509939C-8GENICpossibly homozygous756208411