chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
88189196181891962TC16GENIChomozygous581352964
88189237981892380AG30GENICpossibly homozygous581352965
88189242981892430CT7GENIChomozygous581352966
88189244081892441GA7GENICpossibly homozygous581352967
88189248581892486CT11GENICheterozygous581352968
88189248681892487CG10GENICheterozygous581352969
88189283281892833TC9GENIChomozygous581352970
88189287681892877AG9GENICpossibly homozygous581352971
88189289581892896AC13GENICheterozygous581352972
88189302681893027GA24GENICpossibly homozygous581352973
88189422781894228AG30GENICpossibly homozygous581352974
88189431381894314CA21GENIChomozygous579800628
88189686981896870TC20GENIChomozygous581352975
88189747481897475CG22GENICpossibly homozygous581352976
88189765181897652TC11GENIChomozygous581352977
88189767281897673TC12GENICheterozygous581352978
88189786281897863CT18GENIChomozygous581352979