chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132592959225929593GC35GENIChomozygous809011955
132593001425930015CG48GENIChomozygous809011956
132593147225931473TC34GENIChomozygous809011957
132593148725931488GA30GENIChomozygous809011958
132593149725931498AG36GENICpossibly homozygous809011959
132593152525931526AC29GENICpossibly homozygous809011960
132593154225931543CA26GENICpossibly homozygous809011961
132593209825932099AG41GENIChomozygous809011962
132593396825933969AG33GENIChomozygous809011963
132593445525934456TA61GENICheterozygous809011964
132593445725934458TA62GENICheterozygous809011965
132593470925934710GT59GENIChomozygous809011966
132593570825935709CT51GENIChomozygous809011967
132593592225935923GA59GENIChomozygous809011968
132593697225936973CG23GENICheterozygous809011969
132593698325936984CT22GENICpossibly homozygous809011970
132593969025939691CT55GENIChomozygous809011971
132593998125939982CG43GENIChomozygous809011972
132594018025940181CA50GENIChomozygous809011973
132594036925940370GA42GENIChomozygous809011974
132594109525941096TC52GENIChomozygous809011975
132594119525941196CA32GENIChomozygous809011976
132594120825941209CT32GENIChomozygous809011977
132594173625941737AG60GENICpossibly homozygous809011978
132594208425942085CT35GENIChomozygous809011979
132594308125943082GA87GENIChomozygous809011980
132594554825945549CT61GENIChomozygous809011981
132594768325947684CG26GENIChomozygous809011982
132594982425949825TA46GENIChomozygous809011983