chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4180916181180916182AG36GENICpossibly homozygous112975906
4180916632180916633GA22GENICpossibly homozygous112975907
4180917286180917287AG28GENIChomozygous112975908
4180918858180918859GA21GENICpossibly homozygous112975909
4180919301180919302GA15GENIChomozygous112975910
4180919929180919930TG22GENIChomozygous112975912
4180920599180920600AG20GENICpossibly homozygous113409421
4180922552180922553CG15GENIChomozygous112975915
4180923054180923055GA30GENICpossibly homozygous112975916
4180924344180924345AG32GENIChomozygous112975917
4180930156180930157GA23GENIChomozygous119590922
4180931436180931437TC33GENICpossibly homozygous112975922
4180931821180931822GA35GENICpossibly homozygous112975923
4180931870180931871CT22GENICpossibly homozygous112975924
4180936968180936969CT20GENIChomozygous112975926