chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094064264094065AG30GENICpossibly homozygous810783310
1264094170264094171GT28GENIChomozygous810783311
1264094261264094262TC21GENIChomozygous810783312
1264094954264094955GA30GENIChomozygous810783313
1264095002264095003TC29GENIChomozygous810783314
1264095870264095871CT29GENIChomozygous810783315
1264095886264095887AG34GENIChomozygous810783316
1264096067264096068CG31GENIChomozygous810783317
1264096802264096803GA38GENIChomozygous810783318
1264096893264096894CA28GENIChomozygous810783319
1264096989264096990AG16GENIChomozygous810783320
1264097432264097433TC36GENIChomozygous810783321
1264097484264097485TC37GENIChomozygous810783322
1264097567264097568GA24GENIChomozygous810783323
1264097573264097574GC24GENIChomozygous810783324
1264097633264097634AC29GENIChomozygous810783325
1264097768264097769AG38GENIChomozygous810783326
1264097829264097830TC39GENIChomozygous810783327
1264097921264097922AC26GENIChomozygous810783328
1264097923264097924AT28GENIChomozygous810783329
1264098124264098125TC29GENIChomozygous810783330
1264098178264098179GA21GENIChomozygous810783331
1264098215264098216TC17GENIChomozygous810783332
1264098630264098631AG28GENICpossibly homozygous810783333
1264098735264098736CG57GENICheterozygous810783334
1264099322264099323TC31GENIChomozygous810783335
1264099341264099342AG34GENIChomozygous810783336
1264099343264099344AC36GENIChomozygous810783337
1264099366264099367GA37GENIChomozygous810783338
1264099541264099542GA30GENIChomozygous810783339
1264100050264100051GC28GENIChomozygous810783340
1264100146264100147TC6GENIChomozygous810783341
1264100637264100638TC25GENIChomozygous810783342
1264100900264100901TG32GENIChomozygous810783343
1264101309264101310CT25GENICheterozygous810783344
1264103344264103345CT17GENIChomozygous810783345
1264103826264103827GT26GENIChomozygous810783346