chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91116980511169805G18GENIChomozygous128679280
91116985011169850T13GENIChomozygous128679281
91116986011169860G14GENIChomozygous128679282
91116986311169863T15GENIChomozygous128679283
91116989211169892T12GENIChomozygous128679284
91116989811169898T12GENIChomozygous128679285
91116993511169935G9GENIChomozygous128679286
91116998111169981A19GENIChomozygous128679287
91116999211169992T20GENIChomozygous128679288
91117247011172470T15GENICpossibly homozygous128679289
91118304111183041G7GENIChomozygous128679290
91118362811183628A20GENIChomozygous128679292
91118363311183634C20GENIChomozygous128679293
91118363511183636C21GENIChomozygous128679294
91118363911183639T22GENIChomozygous128679295
91118364011183640TT23GENIChomozygous128679296
91120251811202518GTTTTGGACTGTAAGGGTACTACTCATGAAACGACTATCTCCCAAAGGCCCCGCCTCTGAGAACCATTACACTAGGAAGCAGAACCTCAACAGGCCACATTTAGACCACAATGTTGTGCACCTCATA16GENICpossibly homozygous129957351
91120435111204351GACA28GENIChomozygous128679297
91120373911203739A11GENICheterozygous130571513