chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172354779823547799AG5GENIChomozygous140081590
172354787523547875T19GENIChomozygous140015626
172354820023548200A17GENICpossibly homozygous140015627
172355000223550003AG27GENIChomozygous140081591
172355119823551199AG31GENIChomozygous140081592
172355221923552220GA30GENIChomozygous140081593
172355234123552342CT22GENIChomozygous140081594
172355279123552792CA20GENIChomozygous140081595
172355317023553171TC25GENIChomozygous140081596
172355370523553706TA18GENIChomozygous140081597
172355575623555757GA15GENIChomozygous140081598
172355686923556870GT20GENIChomozygous140081599
172355730023557304GGAA2GENIChomozygous140015628
172355946823559469CG19GENIChomozygous140081600
172355991223559924GAGTTGAAAACC19GENIChomozygous140015630
172356197223561973CT21GENIChomozygous140081601
172356209923562100GA23GENIChomozygous140081602
172356388423563885GC31GENIChomozygous140081603
172356570823565708G18GENIChomozygous140015631
172356715923567160GA32GENIChomozygous140081604
172356762023567621GC42GENIChomozygous140081605
172356933723569338TG30GENIChomozygous140081606
172357099523570995TG9GENICheterozygous140015632
172357142323571424TG17GENIChomozygous140081607
172357293723572938AG21GENIChomozygous140081608
172357604823576049CT27GENIChomozygous140081609
172358207423582075CT20GENIChomozygous140081610
172358236223582363AG27GENIChomozygous140081611
172358253223582533GC23GENIChomozygous140081612
172358269523582696TC23GENIChomozygous140081613
172358271423582715CT25GENIChomozygous140081614
172358332323583324TA21GENIChomozygous140081615
172358411723584118TC22GENIChomozygous140081616
172358445123584452AT22GENIChomozygous140081617
172358458623584587T16GENIChomozygous140015633
172356879823568799TA24GENICheterozygous155023181
172356879823568799TG24GENIChomozygous155023182
172356303123563032TC11GENIChomozygous403410326