chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157247631157247632GT33GENIChomozygous114069291
5157248770157248771AC28GENIChomozygous114452250
5157248814157248815GA28GENIChomozygous114452252
5157249288157249289AG39GENIChomozygous114069292
5157249468157249469CT18GENIChomozygous114452254
5157250146157250147CT37GENIChomozygous114452256
5157251501157251502CA37GENIChomozygous114452258
5157251617157251618AG30GENICpossibly homozygous114452260
5157251778157251779AC26GENIChomozygous114069296
5157251953157251954TC34GENIChomozygous114069297
5157252251157252252TC41GENICpossibly homozygous114452262
5157252798157252799CT29GENIChomozygous114452264
5157252817157252818TA30GENIChomozygous114069298
5157252823157252824TC31GENIChomozygous114069299
5157254282157254283AG27GENIChomozygous114452266
5157254331157254332AC32GENIChomozygous114452268
5157254586157254587TC28GENIChomozygous114069305
5157254587157254588GA29GENIChomozygous114069306
5157254596157254597CA28GENIChomozygous114452270
5157254618157254619TG27GENIChomozygous114452272
5157255053157255054CT29GENICheterozygous114544656
5157255085157255086CT37GENICheterozygous114544658
5157255531157255532GA46GENIChomozygous114069309
5157255825157255826AG36GENIChomozygous114452274
5157256788157256789AT40GENICpossibly homozygous114452276
5157257112157257113GA24GENICheterozygous114069312
5157259659157259660AC43GENIChomozygous114069314
5157261761157261762AC38GENIChomozygous114452278
5157262378157262379AG41GENIChomozygous114069316
5157255059157255060AT35GENICheterozygous114159137
5157268052157268053TC28GENIChomozygous114069326