chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86338155663381557TC7GENIChomozygous116839415
86338658863386589GT7GENIChomozygous116839417
86338686663386867AG32GENIChomozygous116839419
86338935563389356GA17GENIChomozygous116839423
86338962163389622AC14GENIChomozygous116839425
86339157963391580AG10GENIChomozygous116839427
86339163863391639GA19GENIChomozygous116839429
86339209863392099TG13GENIChomozygous116839431
86340132463401325GC18GENIChomozygous116518144
86340252263402523TC10GENIChomozygous116839435
86340622963406230AG27GENIChomozygous116839441
86340774663407747TA15GENIChomozygous116839443
86340784863407849GA8GENIChomozygous116839445
86340974763409748AG18GENIChomozygous116839447
86341182463411825GC12GENIChomozygous116839449
86341624763416248TC16GENIChomozygous116839451
86341795563417956GA10GENIChomozygous116839453
86342067063420671TC19GENIChomozygous116839455
86342154263421543GA10GENIChomozygous116839457
86342256463422565GA22GENIChomozygous116839461
86342511563425116CT10GENIChomozygous116839463
86342626063426261CA9GENICheterozygous116839465
86342653663426537TC21GENIChomozygous116839467
86342806563428066TC18GENIChomozygous116839469
86342822863428229CA16GENIChomozygous116839471
86343022763430228AC17GENIChomozygous116839473
86343232563432326CT18GENIChomozygous116839477
86343257963432580TC18GENIChomozygous116839479
86343358563433586GA19GENIChomozygous116839481
86343564463435645GA17GENIChomozygous116839485
86343767763437678AG29GENIChomozygous116839487
86343900563439006CT25GENIChomozygous116839489
86343934363439344TC5GENIChomozygous116839493
86343947563439476GA13GENIChomozygous116839495
86344057263440573TC17GENIChomozygous116839497
86344092363440924AG17GENIChomozygous116839499
86344399163443992TA19GENIChomozygous116839501
86338671163386712TA7GENIChomozygous126685984
86340441363404414CA17GENIChomozygous126668186
86343361963433620TC19GENIChomozygous126668187