chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172143123021431231GA26GENIChomozygous110987648
172143131821431319AC16GENIChomozygous110987650
172143148721431488AC29GENIChomozygous110987652
172143172021431721CT22GENIChomozygous110987654
172143354521433546TC25GENIChomozygous110987656
172143356621433567CT28GENIChomozygous110987658
172143659921436600GA32GENIChomozygous110987660
172143724121437242GA30GENIChomozygous111413338
172143726221437263TA35GENIChomozygous110987664
172143838421438385CT25GENIChomozygous110987667
172143888921438890GA21GENIChomozygous110987669
172143895021438951AG14GENIChomozygous110987671
172143909221439093CG8GENIChomozygous110987673
172144074921440750GA23GENIChomozygous110987675
172144189921441900TC25GENIChomozygous110987677
172144293321442934GA25GENIChomozygous110987679
172144317821443179CA22GENIChomozygous110987681
172144390421443905GT26GENIChomozygous110987683
172144529521445296AC18GENIChomozygous110987685
172144529621445297CA18GENIChomozygous110987687
172144660021446601GA19GENIChomozygous110987689
172144742721447428GA33GENIChomozygous111413340
172144776521447766TC26GENIChomozygous111298508
172144793521447936TC23GENIChomozygous111338417
172144796621447967GA18GENIChomozygous111338419
172145011921450120TC26GENIChomozygous111338440
172145012821450129TC25GENIChomozygous111338441
172145522921455230TG21GENIChomozygous111413342
172145668521456686AG25GENIChomozygous111298517
172146192021461921AT31GENIChomozygous111413344
172146805321468054TC24GENIChomozygous110987762
172147560221475603AG18GENIChomozygous111178031
172148214021482141GA13GENIChomozygous111413350