chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95655587356555874TC37GENIChomozygous138600321
95655604256556043TA53GENIChomozygous138600322
95655637856556379TC47GENIChomozygous147407880
95655638856556389CT49GENIChomozygous147407881
95655645256556453CT49GENIChomozygous138600323
95655713856557139CT56GENIChomozygous147407882
95655740356557404GC28GENIChomozygous147407883
95655749756557513CGAACCCAGGGCCTTG28GENIChomozygous138465543
95655836256558363CT49GENIChomozygous147407884
95655933956559340TC54GENIChomozygous147407885
95655950456559505AG42GENIChomozygous147407886
95656235656562357TG40GENICpossibly homozygous147407887
95656298556562986AG26GENIChomozygous138600338
95656298956562990GA26GENIChomozygous147407888
95656938756569388CT39GENIChomozygous147407889
95656986456569865TC17GENICpossibly homozygous147407890
95657033056570331CT51GENIChomozygous138600345
95657087656570877GC56GENIChomozygous138600347
95657150556571506GA46GENIChomozygous138600349
95657231756572318CT58GENIChomozygous147407891
95657247856572479AT48GENIChomozygous147407892
95655791956557919TTATTTACAT42GENIChomozygous147406781
95656373556563736A35GENICpossibly homozygous138465550
95656572456565728TTGT40GENIChomozygous147406782
95656986256569863C16GENICpossibly homozygous138465554