chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144578570144578570A15GENIChomozygous128250068
5144578572144578573GA15GENIChomozygous119241483
5144579106144579106T4GENIChomozygous128250069
5144579147144579148C15GENIChomozygous128250070
5144595002144595003AG4GENIChomozygous126205657
5144598386144598388GG15GENIChomozygous128250071
5144581359144581360GT35GENIChomozygous114037451
5144582641144582642CA27GENIChomozygous114037452
5144598389144598390G15GENIChomozygous128250072
5144600435144600436GA17GENIChomozygous114037454
5144600974144600975CT22GENIChomozygous114037455
5144604846144604850TAAA22GENIChomozygous128250073
5144605215144605216TC19GENIChomozygous114037460
5144605602144605602GG23GENIChomozygous128250074
5144607899144607900CT9GENIChomozygous114037461
5144608303144608304T18GENICpossibly homozygous128250075
5144609035144609036GA17GENIChomozygous114037462
5144609863144609863CGAGCC15GENIChomozygous128250076
5144611073144611074TC22GENIChomozygous114037463
5144612867144612868TC6GENIChomozygous126205658
5144604107144604108TA15GENIChomozygous118846264