chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85399005953990060AG29GENICpossibly homozygous67997600
85399047553990476CT30GENIChomozygous67997603
85399187953991880GC25GENIChomozygous67997606
85399200353992004TA37GENIChomozygous67997610
85399220053992201TC34GENIChomozygous67997613
85399360653993607AG25GENIChomozygous67997620
85399420953994210CT13GENIChomozygous67997624
85399475453994755TC19GENICpossibly homozygous67997627
85399959353999594AC38GENIChomozygous67997630
85399489053994891CG32GENIChomozygous69277694
85400082654000827CT32GENIChomozygous69398562
85400082754000828TC31GENIChomozygous69398563
85400181754001818GA29GENIChomozygous67997658
85400278354002784CG40GENIChomozygous67997665
85400392454003925TA38GENIChomozygous67997669
85400656954006570TC17GENICheterozygous69353372
85400657154006572TC16GENICheterozygous69353376
85400659554006596CT15GENIChomozygous67997680
85400816854008169AT36GENIChomozygous67997683
85400845754008458AC19GENICpossibly homozygous67997686
85400886354008864GA41GENIChomozygous67997689
85400987354009874AT28GENIChomozygous67997692
85401001254010013GA37GENIChomozygous67997695