chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172354779823547799AG14GENIChomozygous140081590
172354787523547875T29GENIChomozygous140015626
172354820023548200A34GENIChomozygous140015627
172355000223550003AG51GENIChomozygous140081591
172355119823551199AG71GENIChomozygous140081592
172355221923552220GA59GENIChomozygous140081593
172355234123552342CT67GENIChomozygous140081594
172355279123552792CA59GENIChomozygous140081595
172355317023553171TC46GENIChomozygous140081596
172355370523553706TA50GENIChomozygous140081597
172355575623555757GA61GENIChomozygous140081598
172355686923556870GT36GENIChomozygous140081599
172355730023557304GGAA7GENIChomozygous140015628
172355737423557383GGAAGGGAA13GENIChomozygous140015629
172355946823559469CG53GENIChomozygous140081600
172355991223559924GAGTTGAAAACC48GENIChomozygous140015630
172356197223561973CT68GENIChomozygous140081601
172356209923562100GA64GENIChomozygous140081602
172356388423563885GC45GENIChomozygous140081603
172356570823565708G54GENIChomozygous140015631
172356715923567160GA66GENIChomozygous140081604
172356762023567621GC47GENIChomozygous140081605
172356933723569338TG53GENIChomozygous140081606
172357099523570995TG33GENICpossibly homozygous140015632
172357142323571424TG71GENIChomozygous140081607
172357293723572938AG65GENIChomozygous140081608
172357604823576049CT61GENIChomozygous140081609
172358207423582075CT54GENIChomozygous140081610
172358236223582363AG52GENIChomozygous140081611
172358253223582533GC73GENIChomozygous140081612
172358269523582696TC50GENIChomozygous140081613
172358271423582715CT47GENIChomozygous140081614
172358332323583324TA48GENIChomozygous140081615
172358411723584118TC47GENIChomozygous140081616
172358445123584452AT55GENIChomozygous140081617
172358458623584587T53GENIChomozygous140015633