chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46901298869012989TA22GENIChomozygous71537746
46901319669013197CT25GENIChomozygous70798263
46901325669013257CG28GENIChomozygous71537748
46901341569013416CA28GENIChomozygous71537750
46901341669013417CT30GENIChomozygous71537752
46901352169013522AG19GENIChomozygous71537754
46901362869013629AG23GENIChomozygous71537755
46901375069013751CT26GENIChomozygous71537757
46901384969013850CA15GENIChomozygous71990646
46901399069013991CA25GENIChomozygous71537759
46901408969014090AC25GENIChomozygous71537763
46901418969014190CA17GENIChomozygous71990648
46901421369014214CG14GENIChomozygous71537765
46901504169015042AG33GENIChomozygous71537775
46901514469015145GA58GENICpossibly homozygous71537777