chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10102992136102992137CT5GENIChomozygous591691260
10102992276102992277AG8GENIChomozygous590039612
10102992355102992356AG11GENICpossibly homozygous590039613
10102992762102992763AG8GENIChomozygous590039614
10102993868102993869GA2GENIChomozygous590039615
10102994502102994503CT15GENIChomozygous591691261
10102994923102994924GA12GENICheterozygous590039616
10102995477102995478CT5GENIChomozygous591691262
10102996462102996463CA9GENIChomozygous591691263
10102996527102996528AG16GENIChomozygous591691264
10102996705102996706TC5GENICheterozygous591691265
10102996870102996871GA11GENICpossibly homozygous591691266
10102997159102997160AG13GENIChomozygous591691267
10102997331102997332AC15GENICpossibly homozygous591691268
10102997680102997681AG7GENIChomozygous591691269
10102997726102997727CG4GENICheterozygous590039617
10102997731102997732CT2GENIChomozygous590039618
10102997752102997753C-1GENIChomozygous723354227
10102997775102997776TC1GENIChomozygous591691270
10102997778102997779A-1GENIChomozygous723354228
10102997783102997784CA2GENIChomozygous591691271
10102997785102997786TC4GENIChomozygous591691272
10102997879102997880TC1GENIChomozygous590039619
10102998063102998064CA9GENICpossibly homozygous591691273
10102999026102999027TC3GENIChomozygous591691274
10102999154102999155TTC15GENICpossibly homozygous723354229
10102999439102999440CT22GENIChomozygous591691275