chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69153434091534341GA16GENIChomozygous114898591
69153672791536728GA18GENIChomozygous114898595
69153762791537628TC19GENIChomozygous114898599
69153830891538309CT13GENIChomozygous114898601
69154034891540349AT4GENICheterozygous114898603
69154043791540438TC21GENIChomozygous114898605
69154355391543554CT12GENIChomozygous114898609
69154358491543585TG10GENIChomozygous115503448
69154358591543586CT11GENIChomozygous115503449
69154653191546532AG25GENIChomozygous114898611
69154740991547410AG17GENIChomozygous114898613
69154801991548020CT8GENIChomozygous114898615
69154888691548887GA22GENIChomozygous114898617
69155062991550630CT15GENICheterozygous114898619
69155180791551808TC15GENIChomozygous114898629
69155211991552120GT18GENIChomozygous114898631
69155214591552146AG12GENIChomozygous114898633
69155278191552782TG11GENIChomozygous114898635
69155460691554607AG11GENIChomozygous114898639
69155642691556427TC5GENICheterozygous126436435
69155629691556297CT3GENICheterozygous126436431
69155629791556298AG3GENICheterozygous126436433
69155853891558539CT6GENIChomozygous114898643
69156374591563746GA26GENIChomozygous114898649
69156600491566005TC16GENIChomozygous114898651
69156844391568444AG14GENIChomozygous114898661
69156933991569340CT11GENIChomozygous114898663
69156994291569943CA24GENIChomozygous114898665
69157026191570262GC6GENICheterozygous126418050
69156021791560218GT9GENIChomozygous126372207
69156025591560256GT21GENICpossibly homozygous126357981
69156041091560411GT21GENIChomozygous126357983
69156045691560457GC11GENIChomozygous126357985
69156047091560471GT11GENIChomozygous126357987
69158016891580169CG8GENIChomozygous114898683
69158319791583198GA25GENIChomozygous114898687