chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4211496547211496548GC18GENIChomozygous59861915
4211497759211497760GA31GENIChomozygous57612424
4211497817211497818GC23GENIChomozygous59861917
4211497963211497964CT21GENIChomozygous59861919
4211497985211497986CT14GENIChomozygous59861921
4211497990211497991TA16GENIChomozygous59861923
4211499075211499076AATGTGTG13GENICheterozygous58488365
4211499075211499076AATG13GENICheterozygous58447571
4211499645211499646A-26GENIChomozygous59861925
4211499756211499757AG22GENICpossibly homozygous59861927
4211499770211499771TA22GENICpossibly homozygous59861929
4211500123211500124GC16GENIChomozygous59861932
4211500309211500310CT24GENICpossibly homozygous59861934
4211499140211499142TG--13GENIChomozygous58410747