chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69153434091534341GA13GENIChomozygous114898591
69153672791536728GA16GENIChomozygous114898595
69153762791537628TC24GENIChomozygous114898599
69153830891538309CT26GENIChomozygous114898601
69154043791540438TC18GENIChomozygous114898605
69154355391543554CT19GENIChomozygous114898609
69154358491543585TG19GENIChomozygous115503448
69154358591543586CT20GENIChomozygous115503449
69154653191546532AG22GENIChomozygous114898611
69154740991547410AG28GENIChomozygous114898613
69154801991548020CT26GENIChomozygous114898615
69154888691548887GA25GENIChomozygous114898617
69155211991552120GT24GENIChomozygous114898631
69155214591552146AG24GENIChomozygous114898633
69155278191552782TG13GENIChomozygous114898635
69155460691554607AG18GENIChomozygous114898639
69155853891558539CT24GENIChomozygous114898643
69156019991560200GT10GENIChomozygous114898645
69156020091560201GC10GENIChomozygous114898647
69156374591563746GA24GENIChomozygous114898649
69156600491566005TC30GENIChomozygous114898651
69156712791567128TG23GENIChomozygous114898653
69156713091567131TG23GENIChomozygous114898655
69156713691567137CG23GENIChomozygous114898657
69156713991567140CG24GENIChomozygous114898659
69156844391568444AG14GENIChomozygous114898661
69156933991569340CT22GENIChomozygous114898663
69156994291569943CA21GENIChomozygous114898665
69158016891580169CG22GENIChomozygous114898683
69158319791583198GA17GENIChomozygous114898687