chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152330313123303132CCT18GENICpossibly homozygous48258237
152330527123305272TG24GENIChomozygous48258245
152330623623306237GA7GENIChomozygous48258246
152330628423306285AC4GENIChomozygous48258247
152330674423306745CT25GENIChomozygous48810933
152330680823306809TC23GENIChomozygous48258248
152330916523309168GAC---18GENICpossibly homozygous48258252
152331019623310197A-20GENIChomozygous48258254
152331085423310855TC16GENIChomozygous48258256
152331184523311846CT23GENIChomozygous48258258
152331188423311885CT18GENIChomozygous48258259
152331194523311946TC15GENIChomozygous48258260
152331206123312062GT28GENICpossibly homozygous48810935
152331213823312139AG31GENIChomozygous48810937
152331238123312382GA14GENIChomozygous48258261
152331299523312996CA27GENIChomozygous48258265
152331313023313131TG28GENIChomozygous48258266
152331313323313134G-27GENIChomozygous48258267
152331330423313308CTAA----14GENIChomozygous48810939
152331334823313349TC22GENIChomozygous48258268
152331346123313462GA28GENIChomozygous48258269
152331346323313464GA28GENIChomozygous48258270
152331381023313811AG28GENIChomozygous48258272
152331392223313923TC38GENIChomozygous48258274
152331494923314950GT45GENIChomozygous48810941