chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5121211996121211997CA22GENIChomozygous137605324
5121212271121212272CT26GENICpossibly homozygous137605325
5121213362121213363TC25GENIChomozygous137605326
5121213408121213409GT23GENIChomozygous137605327
5121215436121215437C19GENIChomozygous137337464
5121217351121217352GA24GENIChomozygous137605328
5121220511121220512GC15GENIChomozygous137605329
5121221227121221228AG21GENIChomozygous137605330
5121222495121222496GA10GENIChomozygous137605331
5121222812121222813TC25GENIChomozygous137605332
5121223018121223018AAACA15GENIChomozygous137337465
5121227733121227734TA21GENICpossibly homozygous137605333
5121228597121228598C8GENIChomozygous137337466
5121229116121229117CT5GENIChomozygous137605334
5121229961121229961T19GENIChomozygous137337472
5121230286121230287GA15GENIChomozygous137605335
5121230318121230319GA14GENIChomozygous137605336
5121230645121230646TG16GENIChomozygous137605337
5121231243121231244GA22GENIChomozygous137605338
5121232115121232116A12GENIChomozygous137337473
5121232221121232222G22GENIChomozygous137337474
5121232472121232472G12GENIChomozygous137337475
5121233478121233479GT20GENIChomozygous137605339
5121232115121232116AG12GENICheterozygous154330647