chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173062532130625322CT9GENIChomozygous111023218
173063004130630042AG19GENIChomozygous111023220
173064019930640200GA18GENIChomozygous111023222
173064035330640354CT27GENIChomozygous111023224
173064146830641469AG23GENIChomozygous111023226
173064217230642173AG22GENIChomozygous111023228
173064251430642515GA15GENIChomozygous111023230
173064306230643063AG15GENIChomozygous111023232
173064334430643345TC18GENIChomozygous111023234
173064413630644137GA22GENIChomozygous111023236
173064416730644168AG21GENIChomozygous111023238
173064455130644552CT9GENIChomozygous111023240
173064480130644802AG20GENIChomozygous111023242
173064484330644844TC23GENIChomozygous111023244
173064499530644996AG15GENIChomozygous111023246
173064510130645102TC5GENIChomozygous111399845
173064532930645330GT18GENIChomozygous111023248
173064550230645503AC13GENIChomozygous111023250
173064607230646073TC19GENIChomozygous111399846
173064610030646101AC19GENIChomozygous111023252
173064655930646560AG28GENIChomozygous111023254
173064707030647071TC19GENIChomozygous111023256
173064722630647227CT9GENIChomozygous111023258
173064821030648211AG22GENIChomozygous111023262
173064868030648681GA26GENIChomozygous111023264
173064916730649168GC13GENIChomozygous111023266
173064923330649234TG16GENIChomozygous111023268
173064930830649309TC13GENIChomozygous111023270
173065012130650122CT26GENIChomozygous111023272
173065044330650444AG25GENIChomozygous111023274
173065098830650989TC23GENIChomozygous111023276
173065161230651613CT20GENIChomozygous111023278
173065350530653506AG18GENIChomozygous111023280
173065379030653791CA17GENIChomozygous111023282
173065385130653852GA23GENIChomozygous111023284
173065391930653920TC19GENIChomozygous111023286
173065601130656012GA15GENIChomozygous111023288
173065676630656767GA16GENIChomozygous111023290
173065921330659214AG26GENIChomozygous111023292
173065941830659419GA25GENIChomozygous111023294
173066133030661331AG16GENIChomozygous111023296
173066136230661363AG18GENIChomozygous111023298