chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18484411284844113CT15GENIChomozygous61453822
18484432984844330AG24GENICpossibly homozygous61453823
18484466084844661CT12GENICheterozygous61453824
18484934984849350TC19GENICpossibly homozygous61453826
18484956984849570GC22GENIChomozygous61453827
18484975384849754AG15GENICpossibly homozygous61453828
18484988284849883TTCCCC2GENIChomozygous62551976
18485073184850732AG18GENICpossibly homozygous61453829
18485077584850776CT18GENIChomozygous61453830
18485119884851199AG14GENIChomozygous61453831
18485345184853452AG7GENICheterozygous61453832
18485377684853777TC17GENIChomozygous61453833