chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
54054979940549800CCAA23GENICpossibly homozygous55325282
54054979940549800CCA23GENICheterozygous55325284
54054982140549822GGA18GENIChomozygous55325286
54055205340552054TC46GENIChomozygous55325288
54055208340552084A-32GENIChomozygous55325290
54055253840552539AG24GENIChomozygous55325292
54055354040553543ATA---33GENIChomozygous55325294
54055436140554362A-12GENICheterozygous55325296
54055441640554417AG31GENIChomozygous55325298
54055493440554935CCAAA5GENIChomozygous55325300
54055507840555080AA--19GENICheterozygous55325302
54055507940555080A-19GENICheterozygous55325304
54055539340555394CA23GENICpossibly homozygous55325306
54055594240555943AATAT28GENIChomozygous55325308
54055631140556312A-19GENIChomozygous55325310
54055640840556409GGTTTCTGCCAAGA16GENIChomozygous55325312
54055641040556411AT21GENICheterozygous55325314
54055683640556837TC13GENIChomozygous55325316
54055726940557270GT21GENICpossibly homozygous55325318
54055756940557574GAACC-----15GENICheterozygous55325320
54055759940557604CCTTT-----17GENICheterozygous55325322
54055760540557606A-5GENICheterozygous55325324