chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148137271581372716GT19GENICpossibly homozygous118703742
148140545781405458AT52GENIChomozygous113501560
148142013781420138AG38GENIChomozygous118703744
148142014681420147GT37GENIChomozygous113603633
148142015781420158GA38GENIChomozygous118703745
148142016181420162TA38GENIChomozygous113603634
148142017681420177TG39GENIChomozygous113603635
148142637681426377TA43GENICheterozygous130696654
148142638181426382TA40GENICheterozygous130696655
148142638681426387GC37GENICheterozygous130696656
148142015081420150T37GENIChomozygous129177980
148140292681402926A22GENICheterozygous130428414