chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108347728583477286CA23GENICpossibly homozygous117371385
108347731083477311TC25GENICpossibly homozygous117371387
108347804683478047TC23GENICpossibly homozygous117371389
108347828683478287GT15GENICheterozygous116898575
108347828783478288AC15GENICheterozygous116898577
108347854283478543AG33GENIChomozygous116661285
108347940383479404TA30GENICpossibly homozygous117371391
108347980383479804GC28GENICpossibly homozygous117371393
108348017583480176CT14GENIChomozygous117371395
108348082883480829GA21GENICpossibly homozygous117371397
108348105383481054AT24GENIChomozygous117371399
108348208083482081GA34GENIChomozygous117371401
108348243583482436AG22GENIChomozygous116661287
108348419083484191GA29GENIChomozygous116661289
108348440983484410AG26GENICpossibly homozygous117371403
108348451483484515CT22GENICpossibly homozygous117371405
108348505283485053AG22GENIChomozygous117371407
108348584983485850TC32GENICpossibly homozygous117371409
108348610583486106CA20GENICpossibly homozygous117371411
108348704883487049GA24GENICpossibly homozygous117371413
108348716283487163GT22GENIChomozygous117371415
108348720983487210AG20GENICpossibly homozygous117371417
108348721783487218AG18GENICpossibly homozygous117371419
108348741283487413AG22GENICpossibly homozygous117371421
108348742083487421GA22GENICpossibly homozygous117371423