chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175734996757349968GA44GENIChomozygous145033343
175735000457350005GT40GENIChomozygous145033344
175735007557350076TG46GENIChomozygous145033345
175735020357350204CT51GENIChomozygous145033346
175735064657350647GC41GENIChomozygous145033347
175735091657350917AG49GENIChomozygous145033348
175735107657351077AG44GENIChomozygous145033349
175735113557351136TC46GENIChomozygous145033350
175735118457351185AT54GENIChomozygous145033351
175735165957351660CT47GENIChomozygous145033352
175735189357351894AG41GENIChomozygous145033353
175735197957351980CT46GENIChomozygous145033354
175735198257351983AC45GENIChomozygous145033355
175735205457352055AG55GENICpossibly homozygous145033356
175735207857352079CG49GENICpossibly homozygous145033357
175735176257351771ATTTATTTA42GENICpossibly homozygous145023129
175735207257352073A53GENICpossibly homozygous145023130
175735177057351771A42GENICpossibly homozygous403417757
175735177057351771AT42GENICheterozygous403417758