chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141170334311703344CT10GENIChomozygous113574757
141170334411703345AG11GENIChomozygous113574758
141170335611703357CT21GENICpossibly homozygous113574759
141170349611703497GT19GENIChomozygous113717739
141170358411703585TC16GENIChomozygous113342976
141170359011703591CT14GENIChomozygous113342978
141170370511703706GA6GENIChomozygous113342980
141170388611703887AG10GENIChomozygous113342984
141170395911703960TG18GENIChomozygous113342986
141170426211704263GA18GENIChomozygous113342988
141170433511704336TC18GENIChomozygous113342990
141170450911704510GA10GENIChomozygous113342992
141170512211705123CT20GENIChomozygous113342994
141170569711705698AC19GENIChomozygous113342996
141170707511707076AG14GENIChomozygous113342998
141170785111707852GA7GENIChomozygous113343000
141170811211708113TG14GENIChomozygous113343002
141170823411708235TA24GENIChomozygous113343004