chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61101648511016486GA26GENIChomozygous114723219
61102050511020506CT26GENIChomozygous118584796
61102089111020892CT37GENIChomozygous118584797
61102367511023676CT30GENIChomozygous114723228
61102370611023707GA28GENIChomozygous118584798
61102684411026845AG16GENIChomozygous118584799
61102705811027059CT21GENIChomozygous118584800
61102731311027314GA24GENIChomozygous118584801
61102731411027315CT25GENIChomozygous118584802
61103011011030111GA22GENIChomozygous114723256
61103388811033889TC8GENIChomozygous114723262
61103418011034181CT18GENICpossibly homozygous118584803
61103555311035554AT19GENIChomozygous114723266
61103798411037985TC10GENIChomozygous118648475
61104122411041225GT21GENIChomozygous114723277
61104128411041285TG15GENIChomozygous114723279
61104145511041456GA26GENIChomozygous118571213
61104145611041457AG26GENIChomozygous118571215
61104150111041502GT21GENIChomozygous114723283
61104164811041649TC21GENIChomozygous114723285
61104169311041694CG26GENIChomozygous114723286
61104600011046001TA40GENIChomozygous118584804
61104621911046220CT22GENIChomozygous118584805
61104624011046241GA22GENIChomozygous118584806
61104699011046991TA32GENIChomozygous114723305
61104705011047051CA22GENIChomozygous114723307
61104706811047069CG20GENIChomozygous114723309
61104709611047097CG21GENIChomozygous114723311
61104715011047151TA18GENIChomozygous114723313
61104756211047563CT16GENIChomozygous118571217
61104756311047564TC17GENIChomozygous118571219
61104814611048147AG18GENIChomozygous114723319
61105192111051922TC28GENIChomozygous114723341
61105336211053363AG38GENIChomozygous114723347
61105626311056264GT19GENIChomozygous114723360
61105765411057655TC14GENIChomozygous118584807
61103803011038031GT5GENIChomozygous115236424
61104169411041695GT26GENIChomozygous115236426
61106021611060217GT21GENIChomozygous114723380