chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4180916181180916182AG10GENIChomozygous112975906
4180916632180916633GA15GENIChomozygous112975907
4180917286180917287AG15GENIChomozygous112975908
4180918858180918859GA19GENIChomozygous112975909
4180919301180919302GA23GENIChomozygous112975910
4180919657180919658GA5GENIChomozygous112975911
4180919929180919930TG18GENIChomozygous112975912
4180922552180922553CG20GENIChomozygous112975915
4180923054180923055GA25GENIChomozygous112975916
4180924344180924345AG10GENICheterozygous112975917
4180930156180930157GA22GENIChomozygous119590922
4180931436180931437TC25GENIChomozygous112975922
4180931821180931822GA22GENIChomozygous112975923
4180931870180931871CT19GENIChomozygous112975924
4180934643180934644CG8GENIChomozygous112975925
4180936968180936969CT14GENIChomozygous112975926
4180938094180938095TC16GENIChomozygous112975928
4180922355180922356GT4GENIChomozygous126083876