chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124790436047904361CT30GENIChomozygous958973397
124790442847904429AG30GENIChomozygous958973398
124790503947905040GC31GENIChomozygous958973399
124790505747905058CT29GENIChomozygous958973400
124790592447905925TC43GENIChomozygous958973401
124790718647907187TC15GENIChomozygous958973402
124790723447907235CT18GENIChomozygous958973403
124790755047907551AG35GENICpossibly homozygous958973404
124790807447908075GA25GENIChomozygous958973405
124790818247908183TC32GENIChomozygous958973406
124790853147908532CT35GENIChomozygous958973407
124790978347909784GT33GENIChomozygous958973408
124791088247910883GA18GENIChomozygous958973409
124791103247911033AG33GENIChomozygous958973410
124791118647911187CT34GENIChomozygous958973411
124791214247912143AG31GENIChomozygous958973412
124791233847912339CT17GENIChomozygous958973413
124791237847912379CT20GENIChomozygous958973414
124791329847913299TC28GENIChomozygous958973415
124791396147913962CA27GENIChomozygous958973416
124791396447913965CA29GENIChomozygous958973417
124791409447914095GA21GENIChomozygous958973418
124791421247914213GA22GENIChomozygous958973419
124791539147915392TC23GENIChomozygous958973420
124791703447917035GA24GENIChomozygous958973421
124791720847917209TC20GENIChomozygous958973422
124791870847918709GC25GENIChomozygous958973423
124791936847919369TC37GENIChomozygous958973424
124791985847919859AC29GENIChomozygous958973425