chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64069910040699101GA26GENIChomozygous886402594
64070313740703138TC13GENIChomozygous886402595
64070320640703207TC5GENIChomozygous886402596
64070356140703562GC14GENIChomozygous886402597
64070400940704010CA20GENIChomozygous886402598
64070436840704369AC6GENIChomozygous886402599
64070448640704487TG19GENIChomozygous886402600
64070587140705872TA21GENIChomozygous886402601
64070641040706411GT21GENIChomozygous886402602
64070653040706531CT16GENIChomozygous886402603
64070716540707166CT17GENIChomozygous886402604
64070747540707476GT20GENIChomozygous886402605
64070749640707497TG25GENIChomozygous886402606
64070879140708792AG19GENIChomozygous886402607
64070914340709144TA15GENIChomozygous886402608
64070915340709154TG19GENIChomozygous886402609
64070977740709778CT9GENIChomozygous886402610
64070977840709779AG9GENIChomozygous886402611
64070985340709854TA17GENICpossibly homozygous886402612
64070985440709855GC17GENIChomozygous886402613
64070988040709881GA19GENIChomozygous886402614
64071041340710414TC19GENIChomozygous886402615
64071068040710681GA4GENIChomozygous886402616
64071176040711761GC3GENICheterozygous886402617
64071209640712097CT25GENIChomozygous886402618
64071250040712501TA15GENIChomozygous886402619
64071331540713316TC6GENIChomozygous886402620
64071333840713339GA12GENIChomozygous886402621