chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150957369150957370CG5GENIChomozygous114540801
5150957860150957861TC14GENIChomozygous114540803
5150958437150958438AG19GENIChomozygous114540805
5150958731150958732TC32GENIChomozygous114540811
5150958997150958998CT26GENIChomozygous114540813
5150959051150959052CT33GENIChomozygous114540815
5150959215150959216TC23GENIChomozygous114540817
5150959438150959439GT35GENIChomozygous114540819
5150959892150959893CA15GENIChomozygous119021270
5150959897150959898GA14GENIChomozygous114350254
5150961285150961286CA33GENIChomozygous114350266
5150962151150962152GA24GENIChomozygous114350274
5150962157150962158AG24GENIChomozygous114350276
5150962519150962520CG16GENIChomozygous114350280
5150962603150962604CT28GENIChomozygous114350282
5150962617150962618CT26GENIChomozygous114350284
5150962873150962874GA28GENIChomozygous114350286
5150963627150963628CT27GENIChomozygous118984020
5150964281150964282TC29GENIChomozygous114350292
5150964529150964530TG21GENIChomozygous114350294
5150964792150964793CG16GENIChomozygous114350296
5150964978150964979CT13GENIChomozygous114350298
5150965003150965004TC13GENIChomozygous114350300
5150965583150965584CT23GENIChomozygous114350302
5150965763150965764TC26GENICpossibly homozygous114350304
5150965916150965917GA24GENIChomozygous114350306
5150965940150965941CT25GENIChomozygous114350308
5150966003150966004GA15GENIChomozygous114350310
5150966680150966681AG20GENIChomozygous114350318
5150966767150966768TC22GENIChomozygous114350322
5150967524150967525GA21GENIChomozygous114350324