chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094064264094065AG58GENIChomozygous978059226
1264094170264094171GT40GENIChomozygous978059227
1264094261264094262TC28GENIChomozygous978059228
1264094954264094955GA22GENIChomozygous978059229
1264095002264095003TC24GENIChomozygous978059230
1264095870264095871CT30GENIChomozygous978059231
1264095886264095887AG30GENIChomozygous978059232
1264096067264096068CG20GENIChomozygous978059233
1264096228264096229CA35GENIChomozygous978059234
1264096229264096230AT35GENIChomozygous978059235
1264096802264096803GA31GENIChomozygous978059236
1264096893264096894CA42GENIChomozygous978059237
1264096989264096990AG29GENICpossibly homozygous978059238
1264097432264097433TC55GENIChomozygous978059239
1264097484264097485TC60GENIChomozygous978059240
1264097567264097568GA44GENIChomozygous978059241
1264097573264097574GC45GENIChomozygous978059242
1264097633264097634AC58GENIChomozygous978059243
1264097768264097769AG48GENIChomozygous978059244
1264097829264097830TC44GENIChomozygous978059245
1264097921264097922AC57GENIChomozygous978059246
1264097923264097924AT57GENIChomozygous978059247
1264098124264098125TC47GENIChomozygous978059248
1264098178264098179GA61GENIChomozygous978059249
1264098215264098216TC47GENIChomozygous978059250
1264099322264099323TC19GENIChomozygous978059251
1264099341264099342AG19GENIChomozygous978059252
1264099343264099344AC18GENIChomozygous978059253
1264099366264099367GA17GENIChomozygous978059254
1264099541264099542GA27GENIChomozygous978059255
1264100050264100051GC23GENIChomozygous978059256
1264100637264100638TC43GENIChomozygous978059257
1264100900264100901TG32GENIChomozygous978059258
1264103344264103345CT32GENIChomozygous978059259