chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144578570144578570A9GENIChomozygous128250068
5144578572144578573GA9GENIChomozygous119241483
5144579106144579106T4GENIChomozygous128250069
5144579147144579148C11GENIChomozygous128250070
5144595002144595003AG4GENIChomozygous126205657
5144598386144598388GG36GENIChomozygous128250071
5144598389144598390G36GENIChomozygous128250072
5144600974144600975CT33GENIChomozygous114037455
5144581359144581360GT41GENIChomozygous114037451
5144582641144582642CA38GENIChomozygous114037452
5144600435144600436GA36GENIChomozygous114037454
5144604107144604108TA20GENICpossibly homozygous118846264
5144604846144604850TAAA46GENIChomozygous128250073
5144605215144605216TC34GENIChomozygous114037460
5144605602144605602GG54GENIChomozygous128250074
5144607899144607900CT30GENIChomozygous114037461
5144608303144608304T37GENICpossibly homozygous128250075
5144609035144609036GA36GENIChomozygous114037462
5144609863144609863CGAGCC37GENIChomozygous128250076
5144611073144611074TC43GENIChomozygous114037463
5144612867144612868TC19GENIChomozygous126205658