chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3106231088106231089TC15GENIChomozygous136782883
3106231278106231279GC23GENIChomozygous136782884
3106231514106231515GC28GENIChomozygous136782885
3106232970106232971CG33GENIChomozygous141524557
3106233310106233311TC32GENIChomozygous136782888
3106233450106233451AG14GENICheterozygous403072904
3106233446106233447A14GENICheterozygous403072899
3106233446106233447AG14GENICheterozygous403072900
3106233448106233449A14GENICheterozygous403072901
3106233448106233449AG14GENICheterozygous403072902
3106233450106233451A14GENICheterozygous403072903
3106233461106233462T14GENICheterozygous403072905
3106233461106233462TG14GENICheterozygous403072906
3106234662106234663TC7GENIChomozygous403072907
3106234662106234663TG7GENICheterozygous403072908
3106234662106234663T7GENICheterozygous403072909
3106235860106235861GA24GENIChomozygous141524558
3106239236106239237GA23GENIChomozygous141524559
3106239291106239292CT21GENIChomozygous141524560
3106240256106240257GC19GENIChomozygous141524561
3106240579106240580A16GENIChomozygous403072910
3106240579106240580AT16GENICheterozygous403072911
3106240622106240623TC18GENIChomozygous136782896
3106240625106240626TC17GENIChomozygous136782897
3106240628106240629TC17GENIChomozygous136782898
3106240631106240632TC16GENIChomozygous136782899
3106240819106240820AG11GENIChomozygous141524562
3106242289106242290TG15GENIChomozygous141524563
3106242434106242435CT21GENIChomozygous141524564
3106242747106242748CT19GENIChomozygous141524565
3106243736106243737AG16GENIChomozygous141524566
3106240649106240650CA16GENIChomozygous144647427
3106233440106233462AGAGAGAGAGAGAGAGAGAGAT13GENICheterozygous141478459
3106236560106236560T23GENIChomozygous141478460
3106242821106242823GA18GENICpossibly homozygous141478461
3106236428106236428GG8GENICheterozygous145133474
3106240616106240617TC19GENIChomozygous144647425
3106240619106240620TC19GENIChomozygous144647426