chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1134787454134787455AG5GENIChomozygous74460417
1134787456134787457AG5GENIChomozygous74460419
1134787468134787469AG4GENIChomozygous74460421
1134791935134791936CG23GENICheterozygous75709790
1134799102134799103AG25GENIChomozygous74460441
1134802643134802644CG28GENICheterozygous74460451
1134807290134807291TG22GENIChomozygous74460483
1134807418134807419CA18GENIChomozygous75133016
1134808124134808125GA28GENIChomozygous75133017
1134808566134808567TC20GENIChomozygous74460489
1134808636134808637AG19GENIChomozygous74460491
1134810642134810643GA24GENIChomozygous74460501
1134811045134811046TC21GENIChomozygous74460503
1134812268134812269AG15GENIChomozygous75133018
1134817203134817204GA26GENIChomozygous75133020
1134818223134818224GA21GENIChomozygous75133021
1134820072134820073TC24GENIChomozygous74460511
1134821745134821746TG24GENIChomozygous74460513
1134822310134822311CG27GENIChomozygous74460515
1134825569134825570CT15GENIChomozygous75133022
1134832972134832973TC23GENIChomozygous74460521
1134835412134835413AT22GENIChomozygous74460525
1134837168134837169TC21GENIChomozygous74460527
1134837392134837393TA24GENIChomozygous75133023
1134838112134838113TG24GENIChomozygous74460529
1134840573134840574CT32GENICheterozygous74460531
1134841937134841938CT24GENIChomozygous74460535
1134842747134842748TC12GENIChomozygous74460537
1134843772134843773GA18GENIChomozygous75133024
1134844840134844841AG23GENIChomozygous74460539
1134846181134846182GA23GENIChomozygous75133025
1134848144134848145AG22GENIChomozygous74460541