chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4180916181180916182AG29GENIChomozygous112975906
4180916632180916633GA19GENIChomozygous112975907
4180917286180917287AG18GENIChomozygous112975908
4180918858180918859GA18GENIChomozygous112975909
4180919301180919302GA16GENIChomozygous112975910
4180919657180919658GA11GENIChomozygous112975911
4180919929180919930TG16GENIChomozygous112975912
4180921920180921921CT4GENICheterozygous112975914
4180922552180922553CG24GENIChomozygous112975915
4180923054180923055GA19GENIChomozygous112975916
4180931436180931437TC13GENIChomozygous112975922
4180931821180931822GA18GENIChomozygous112975923
4180931870180931871CT31GENIChomozygous112975924
4180934643180934644CG7GENIChomozygous112975925
4180936968180936969CT11GENIChomozygous112975926
4180937695180937696GA4GENICheterozygous126121305
4180937709180937710GA5GENICheterozygous112975927
4180938094180938095TC33GENIChomozygous112975928