chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85927900959279010CT56GENIChomozygous116831145
85927947659279477AC44GENIChomozygous116511374
85927976959279770GA59GENIChomozygous116831147
85927987959279880GA43GENIChomozygous116511378
85928044559280446AG50GENIChomozygous116831149
85928055159280552CT50GENIChomozygous116511382
85928063459280635GA56GENIChomozygous116831151
85928072759280728AG55GENIChomozygous116831153
85928096459280965GA67GENIChomozygous116511384
85928247259282473TG41GENIChomozygous116831155
85928340959283410GC52GENIChomozygous116511386
85928351959283520GA55GENIChomozygous116831157
85928456359284564AT66GENIChomozygous116831159
85928505459285055AC62GENICpossibly homozygous116511388
85928510059285101TC55GENIChomozygous116831161
85928612059286121CT55GENIChomozygous116831165
85928700759287008TC51GENIChomozygous116831167
85928735459287355AG48GENIChomozygous116831169
85928762159287622GA17GENIChomozygous116831171
85928762659287627GA18GENICpossibly homozygous116831173
85928773059287731AG51GENIChomozygous116511390
85928810359288104AC55GENIChomozygous116511392
85928815559288156TC57GENIChomozygous116511394
85928838959288390GA47GENIChomozygous116831175
85929172459291725AG64GENIChomozygous116511398
85929176659291767TC69GENIChomozygous116511400
85929236859292369GA52GENIChomozygous116831183
85928168759281688T56GENIChomozygous131048421
85928233659282336CCCACCCT17GENIChomozygous131048422
85928542859285428C26GENIChomozygous130363067