chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3106231088106231089TC27GENIChomozygous136782883
3106231278106231279GC17GENIChomozygous136782884
3106231514106231515GC23GENIChomozygous136782885
3106232970106232971CG28GENIChomozygous141524557
3106233310106233311TC23GENIChomozygous136782888
3106233450106233451A20GENIChomozygous403072903
3106233446106233447A20GENIChomozygous403072899
3106233446106233447AG20GENICheterozygous403072900
3106233448106233449A20GENIChomozygous403072901
3106233448106233449AG20GENICheterozygous403072902
3106233450106233451AG20GENICheterozygous403072904
3106233461106233462T20GENIChomozygous403072905
3106233461106233462TG20GENICheterozygous403072906
3106235860106235861GA17GENIChomozygous141524558
3106239236106239237GA18GENIChomozygous141524559
3106239291106239292CT21GENIChomozygous141524560
3106240256106240257GC20GENIChomozygous141524561
3106240579106240580A8GENIChomozygous403072910
3106240579106240580AT8GENICheterozygous403072911
3106240622106240623TC10GENIChomozygous136782896
3106240625106240626TC10GENIChomozygous136782897
3106240628106240629TC9GENIChomozygous136782898
3106240631106240632TC9GENIChomozygous136782899
3106240649106240650CA12GENIChomozygous144647427
3106236428106236428GG10GENIChomozygous145133474
3106236432106236434TG10GENIChomozygous145133475
3106236560106236560T15GENIChomozygous141478460
3106240616106240617TC10GENIChomozygous144647425
3106240619106240620TC10GENIChomozygous144647426
3106240819106240820AG20GENIChomozygous141524562
3106242289106242290TG18GENICpossibly homozygous141524563
3106242434106242435CT28GENIChomozygous141524564
3106242747106242748CT21GENIChomozygous141524565
3106242821106242823GA23GENIChomozygous141478461
3106243736106243737AG12GENIChomozygous141524566