chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91116980511169805G58GENIChomozygous128679280
91116985011169850T53GENIChomozygous128679281
91116986011169860G54GENIChomozygous128679282
91116986311169863T55GENIChomozygous128679283
91116989211169892T60GENIChomozygous128679284
91116989811169898T58GENIChomozygous128679285
91116993511169935G50GENIChomozygous128679286
91116998111169981A45GENIChomozygous128679287
91116999211169992T49GENIChomozygous128679288
91117247011172470T46GENICpossibly homozygous128679289
91118304111183041G14GENIChomozygous128679290
91118362811183628A29GENIChomozygous128679292
91118363311183634C29GENIChomozygous128679293
91118363511183636C30GENIChomozygous128679294
91118363911183639T30GENIChomozygous128679295
91118364011183640TT32GENIChomozygous128679296
91120435111204351GACA65GENIChomozygous128679297
91120251811202518GTTTTGGACTGTAAGGGTACTACTCATGAAACGACTATCTCCCAAAGGCCCCGCCTCTGAGAACCATTACACTAGGAAGCAGAACCTCAACAGGCCACATTTAGACCACAATGTTGTGCACCTCATA40GENICpossibly homozygous129957351
91120373911203739A36GENICheterozygous130571513