chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13106067519106067520TA6GENIChomozygous114438285
13106166968106166969TC15GENICheterozygous114655224
13106173491106173492TG12GENICheterozygous114655225
13106201595106201596AC16GENIChomozygous114438287
13106247826106247827TA2GENIChomozygous114655226
13106344469106344470AG20GENICpossibly homozygous114438297
13106351465106351466TA8GENIChomozygous114598811
13106351485106351486TG12GENIChomozygous114598813
13106351487106351488TA16GENIChomozygous114598815
13106351489106351490TA17GENIChomozygous114598817
13106351496106351497TC20GENIChomozygous114598819
13106351498106351499TA20GENIChomozygous114598821
13106351500106351501TG20GENIChomozygous114598823
13106369843106369844AG23GENIChomozygous114438299
13106390258106390259TA6GENIChomozygous114438301
13106401053106401054AG15GENIChomozygous114438303
13106401109106401110TC27GENIChomozygous114438305
13106401160106401161CT30GENIChomozygous114438307
13106402081106402082GC34GENIChomozygous114438313
13106434274106434275CT31GENIChomozygous114438315
13106438789106438790GT46GENIChomozygous114438317
13106439073106439074TG29GENICpossibly homozygous114438319
13106542765106542766AT26GENIChomozygous114438323
13106543105106543106AC17GENICheterozygous114655227
13106624528106624529TG20GENICheterozygous114655228
13106627731106627732TA33GENIChomozygous114438325
13106627751106627752GT31GENIChomozygous114438327
13106653116106653117GC15GENICheterozygous114655229
13106658482106658483CT15GENIChomozygous114655230
13106678814106678815GT14GENIChomozygous114599746