chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145472369145472370TC55GENIChomozygous112870906
4145476226145476227CT46GENIChomozygous112870907
4145479279145479280GA44GENIChomozygous112870908
4145472937145472938A37GENIChomozygous128087995
4145480529145480530TC38GENIChomozygous112870909
4145481733145481734CT45GENIChomozygous112870910
4145481748145481749CG43GENIChomozygous112870911
4145484746145484747TC37GENIChomozygous112870913
4145485656145485657CT41GENIChomozygous112870914
4145485793145485794GT30GENIChomozygous112870915
4145485796145485797GT34GENICpossibly homozygous112870916
4145486325145486326GT38GENIChomozygous112870917
4145486784145486785GC37GENIChomozygous112870918
4145486793145486794GC36GENIChomozygous112870919