chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101054017710540178GC77GENIChomozygous116493210
101054059810540599TC72GENIChomozygous116493212
101054067010540671TC73GENIChomozygous116493214
101054193210541933CA61GENIChomozygous116493216
101054236310542364CA57GENIChomozygous116493218
101054244210542443AG48GENIChomozygous116493220
101054270710542708TA33GENIChomozygous116493222
101054422810544229CT65GENIChomozygous116493224
101054454810544549CT62GENIChomozygous116493226
101054632310546324AG73GENIChomozygous116493228
101054765310547654CA63GENIChomozygous116493230
101054777910547780TC59GENIChomozygous116493232
101054807310548074AG49GENIChomozygous116493234
101054835510548356AT57GENIChomozygous116493236
101054886710548868AC74GENIChomozygous116493238
101054895310548954AG58GENIChomozygous116493240
101054934410549345TC76GENIChomozygous116493242
101055003410550035TC71GENIChomozygous116493244
101055007510550076CG74GENIChomozygous116493246
101054596710545967CATGAG55GENIChomozygous128789351
101054960310549603G70GENIChomozygous128789352