chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86775422467754228TGTC41GENICpossibly homozygous133190877
86775445167754452AC41GENIChomozygous117947317
86775499067754991GA27GENIChomozygous117947318
86775526867755272CTTG37GENIChomozygous133190878
86775587767755878AG44GENIChomozygous117947319
86775746967757470TC42GENIChomozygous117947320
86775760467757605TC48GENIChomozygous117947321
86775930567759306TC41GENIChomozygous117947322
86775962067759621AT51GENIChomozygous117947323
86775964767759648TC48GENIChomozygous117947324
86776169667761697CG46GENICpossibly homozygous117947325
86776257667762577AT26GENIChomozygous118027178
86776445067764451TC55GENIChomozygous117947326
86776112167761122GC41GENIChomozygous133414437
86776271567762716GA33GENIChomozygous118099788
86776278667762787GT20GENIChomozygous116520103
86776288967762889A23GENIChomozygous128600137