chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23418717734187178TG20GENIChomozygous110682279
23418764234187643GA13GENIChomozygous110682281
23418783034187831GA24GENIChomozygous110682283
23418842934188430GA28GENIChomozygous110682285
23418877234188773CT36GENIChomozygous110682287
23418878034188781AG33GENIChomozygous109688735
23418951534189516AG20GENIChomozygous110682289
23419004834190049CT31GENIChomozygous110682291
23419462134194622TC31GENIChomozygous110682293
23419505034195051AG24GENIChomozygous110682294
23419550334195504GA40GENIChomozygous110682296
23419568834195689TC29GENIChomozygous109688739
23419665734196658AG22GENIChomozygous110682298
23419874534198746CG37GENIChomozygous110682302
23420364234203643CG41GENIChomozygous110682306
23420472334204724CT34GENIChomozygous110682308
23420600934206010TC26GENIChomozygous109688749
23420861934208620CT38GENIChomozygous110682310
23420993934209940GA14GENIChomozygous109688751
23421036234210363TA24GENIChomozygous109688753
23421251334212514CT26GENIChomozygous109688755
23421320534213206CT37GENIChomozygous109688757
23421371934213720AG42GENICpossibly homozygous109688759
23421403734214038TC40GENIChomozygous109688761
23421426234214263GC34GENIChomozygous109688763
23421492934214930GT46GENIChomozygous109688765
23421659334216594AC20GENIChomozygous109688775
23421729234217293AG19GENIChomozygous120178064
23421737134217372TA18GENIChomozygous109688779
23421751434217515TC25GENIChomozygous109688781
23421777934217780TC26GENIChomozygous109688783
23421783034217831GA32GENIChomozygous109688785
23421790934217910CT29GENIChomozygous109688787
23421791234217913TA28GENIChomozygous109688789
23421793134217932AG28GENIChomozygous109688791
23421793734217938TG32GENIChomozygous109688793
23421821634218217GA25GENIChomozygous109688797
23421821834218219CT25GENIChomozygous109688799
23422080634220807CG41GENIChomozygous109688803
23422190634221907TC27GENIChomozygous110682314