chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108904944289049443CT42GENIChomozygous51731304
108904966789049668CT32GENICheterozygous51731306
108904977289049773TC27GENICheterozygous51731308
108904983389049834CT23GENICpossibly homozygous51731310
108905096689050967GT48GENIChomozygous51731312
108905112489051125TG53GENICpossibly homozygous51731314
108905154089051541GT17GENICpossibly homozygous51536520
108905154289051543CCT14GENIChomozygous51731316
108905154989051550CCA12GENIChomozygous51731318
108905158189051582GA18GENIChomozygous51731320
108905194189051942CT41GENIChomozygous51731322
108905222089052221CT58GENIChomozygous51731324
108905271989052720AG16GENICpossibly homozygous51731328
108905272989052730TC15GENICpossibly homozygous51731330
108905275189052752CT13GENICheterozygous51731332
108905281289052813A-2GENIChomozygous51731334
108905283489052835CG4GENIChomozygous51731336
108905291389052914AAG18GENICpossibly homozygous51731338
108905291689052917AAG19GENICpossibly homozygous51731340
108905291989052920AAG20GENIChomozygous51731342
108905297989052980AAT33GENIChomozygous51731344
108905313289053133AG53GENICpossibly homozygous51731346
108905313789053138CA52GENICpossibly homozygous51731348
108905380589053806GA48GENIChomozygous51731356
108905334189053342TG32GENICheterozygous51731350
108905334189053342TTTTGTTTGG27GENIChomozygous51731352
108905334589053346GT33GENICheterozygous51731354
108905414189054142GA36GENICpossibly homozygous51731358
108905427989054280CT53GENIChomozygous51731360
108905509889055099CT53GENICpossibly homozygous51731362
108905518689055187CT45GENIChomozygous51731364
108905578289055783TC42GENIChomozygous51731366
108905600789056010GTC---38GENIChomozygous51731368
108905717489057175GA56GENICpossibly homozygous51731370