chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3119792098119792099CG43GENIChomozygous57628785
3119792828119792829C-38GENIChomozygous57628787
3119792829119792830CT38GENIChomozygous58994764
3119793236119793238CC--45GENIChomozygous57628789
3119793508119793509AC38GENIChomozygous57628791
3119793724119793725AG46GENIChomozygous57628793
3119794384119794385CT35GENIChomozygous57628795
3119794525119794526G-16GENICpossibly homozygous57628797
3119794646119794647AC52GENIChomozygous57628801
3119794878119794879CT38GENIChomozygous57628803
3119795114119795115G-45GENIChomozygous57628805
3119795397119795398AG52GENIChomozygous57628807
3119795796119795797GA58GENIChomozygous57628809
3119795945119795946GA30GENIChomozygous57628813
3119797586119797587AC39GENIChomozygous57628815
3119798677119798678AG47GENIChomozygous57628817
3119799012119799013GC38GENIChomozygous57628819
3119799169119799170GT41GENIChomozygous57628821
3119799348119799349TG41GENIChomozygous57628823
3119799505119799506AATT8GENIChomozygous58621190
3119799672119799673GGGTGTGTGTGT11GENICheterozygous58692723
3119799672119799673GGGTGTGTGTGTGT11GENICheterozygous59046517
3119803159119803160GA33GENIChomozygous57628829
3119805150119805151TC53GENIChomozygous57628831
3119806236119806237AG45GENICpossibly homozygous57628833
3119807030119807031CT30GENIChomozygous57628835
3119807319119807320GC34GENIChomozygous57628837
3119807788119807789TC31GENIChomozygous57628839
3119808454119808455GA31GENIChomozygous57628841
3119810231119810232AG42GENIChomozygous57628843
3119810537119810538CT42GENIChomozygous57628845
3119811110119811111GA48GENIChomozygous57628847