chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64852992848529929CT22GENIChomozygous137768696
64853107148531072GA25GENIChomozygous137768697
64853177748531778TA17GENIChomozygous137768698
64853247048532471CA17GENIChomozygous137768699
64853261548532616TC19GENIChomozygous137768700
64853487848534878A12GENICheterozygous137680976
64853849248538493GA20GENIChomozygous137768701
64853989248539893TC11GENIChomozygous137768702
64854127048541271GA18GENIChomozygous137768703
64854204148542042GC19GENIChomozygous137768704
64854377748543778AT32GENIChomozygous137768705
64854385248543853T22GENIChomozygous137680977
64854389948543900AG20GENIChomozygous137768706
64854540648545407AG6GENIChomozygous137768707
64854563848545639AC13GENIChomozygous137768708
64854569448545695GA20GENIChomozygous137768709
64854702648547027CT21GENICpossibly homozygous137768710
64854727748547278TC29GENIChomozygous137768711
64854729148547292CT26GENIChomozygous137768712
64854807048548070A9GENIChomozygous137680978
64854915548549156GA19GENIChomozygous137768713
64854960848549609T12GENICheterozygous137680979
64854985748549858AG18GENIChomozygous137768714
64855289248552893GA23GENIChomozygous137768715
64855386248553863TG15GENICpossibly homozygous137768716