chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91116980511169805G44GENIChomozygous128679280
91116985011169850T39GENIChomozygous128679281
91116986011169860G39GENIChomozygous128679282
91116986311169863T39GENIChomozygous128679283
91116989211169892T43GENIChomozygous128679284
91116989811169898T41GENIChomozygous128679285
91116993511169935G44GENIChomozygous128679286
91116998111169981A38GENIChomozygous128679287
91116999211169992T35GENIChomozygous128679288
91117247011172470T34GENICpossibly homozygous128679289
91118304111183041G11GENIChomozygous128679290
91118347111183472C7GENIChomozygous128679291
91118362811183628A35GENIChomozygous128679292
91118363311183634C36GENIChomozygous128679293
91118363511183636C36GENIChomozygous128679294
91118363911183639T35GENIChomozygous128679295
91118364011183640TT33GENIChomozygous128679296
91120435111204351GACA43GENIChomozygous128679297
91120251811202518GTTTTGGACTGTAAGGGTACTACTCATGAAACGACTATCTCCCAAAGGCCCCGCCTCTGAGAACCATTACACTAGGAAGCAGAACCTCAACAGGCCACATTTAGACCACAATGTTGTGCACCTCATA46GENICpossibly homozygous129957351