chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113164321731643218GA34GENIChomozygous116129297
113164751131647514TTG39GENIChomozygous128896236
113165068131650681A21GENIChomozygous128896237
113165154731651548TA31GENIChomozygous115812280
113164542931645430GA22GENIChomozygous115812270
113164601031646011TG32GENIChomozygous115812272
113164622531646226TC28GENIChomozygous115812274
113164663831646639CT35GENIChomozygous115812276
113164693631646937TC37GENICpossibly homozygous115812278
113165170731651707C25GENICpossibly homozygous128896238
113165247631652477GA38GENIChomozygous115812282
113165346131653462TA25GENIChomozygous115812284
113165368831653689GA38GENIChomozygous115812286
113165457131654572AT36GENIChomozygous115812288
113165517831655179GA26GENIChomozygous115812290
113165536531655366AT24GENIChomozygous115812292
113165552131655522GA33GENIChomozygous115812294
113165561531655616TG29GENIChomozygous115812296
113165664231656643AC23GENIChomozygous118141590
113165724331657244GA29GENIChomozygous115812298
113165806831658069CT10GENIChomozygous118141592
113165807131658072GA12GENIChomozygous118141593
113165808531658086GA11GENIChomozygous118141595
113165808931658090GC11GENIChomozygous118141597
113165815231658153G10GENIChomozygous128896239
113165844331658444AG28GENIChomozygous115812300
113166000131660002TC27GENIChomozygous115812302
113166462431664625GC29GENIChomozygous115812304
113166633231666333CT27GENIChomozygous115812308
113165805631658057GA12GENIChomozygous116314288