chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121328464713284648CT7GENIChomozygous115260277
121328477513284776TC19GENIChomozygous115260279
121328491913284920CT20GENIChomozygous115260281
121328496113284962AG16GENIChomozygous115260283
121328532913285330CT27GENIChomozygous115260285
121328751113287512AG16GENIChomozygous115260289
121328821513288216TC23GENIChomozygous126167715
121328830913288310GT18GENIChomozygous126167716
121328833913288340TC14GENIChomozygous126167717
121328836413288365GT11GENIChomozygous126167718
121328938213289383TC15GENIChomozygous115260293
121329011313290114AG23GENIChomozygous115260295
121329104613291047GA21GENIChomozygous115260297
121329122213291223CT17GENICpossibly homozygous115260299
121329165513291656AG12GENIChomozygous115260301
121329166413291665TC8GENIChomozygous115260303
121329191513291916GA27GENIChomozygous115260305
121329345313293454CT5GENICheterozygous126167719
121329421113294212GA10GENICheterozygous118245351
121329634813296349TC24GENIChomozygous115260307
121329722913297230GA27GENIChomozygous126167720
121329740313297404TC22GENIChomozygous126167721
121329743413297435TC18GENIChomozygous126167722
121329764113297642CT18GENIChomozygous115260309
121329789613297897TC11GENIChomozygous115362591
121329795813297959AC5GENICheterozygous126191435