chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141170334311703344CT11GENICheterozygous113574757
141170334411703345AG11GENIChomozygous113574758
141170335611703357CT17GENIChomozygous113574759
141170358411703585TC14GENIChomozygous113342976
141170359011703591CT10GENIChomozygous113342978
141170370511703706GA10GENIChomozygous113342980
141170371411703715CT10GENIChomozygous113342982
141170388611703887AG9GENIChomozygous113342984
141170395911703960TG17GENIChomozygous113342986
141170426211704263GA15GENIChomozygous113342988
141170433511704336TC12GENIChomozygous113342990
141170450911704510GA4GENIChomozygous113342992
141170512211705123CT10GENIChomozygous113342994
141170569711705698AC11GENIChomozygous113342996
141170707511707076AG4GENIChomozygous113342998
141170785111707852GA6GENIChomozygous113343000
141170811211708113TG18GENIChomozygous113343002
141170823411708235TA16GENIChomozygous113343004