chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3106231088106231089TC52GENIChomozygous136782883
3106231278106231279GC54GENIChomozygous136782884
3106231514106231515GC61GENIChomozygous136782885
3106233310106233311TC47GENIChomozygous136782888
3106232970106232971CG50GENIChomozygous141524557
3106233448106233449AG35GENICheterozygous403072902
3106233448106233449A35GENIChomozygous403072901
3106233446106233447A35GENIChomozygous403072899
3106233446106233447AG35GENICheterozygous403072900
3106233450106233451A35GENIChomozygous403072903
3106233450106233451AG35GENICheterozygous403072904
3106233461106233462T35GENIChomozygous403072905
3106233461106233462TG35GENICheterozygous403072906
3106234662106234663TC18GENICpossibly homozygous403072907
3106234662106234663TG18GENICheterozygous403072908
3106234662106234663T18GENICheterozygous403072909
3106235860106235861GA34GENIChomozygous141524558
3106239236106239237GA38GENIChomozygous141524559
3106239291106239292CT49GENIChomozygous141524560
3106240256106240257GC36GENIChomozygous141524561
3106240579106240580A19GENIChomozygous403072910
3106240579106240580AT19GENICheterozygous403072911
3106240622106240623TC25GENIChomozygous136782896
3106240625106240626TC25GENIChomozygous136782897
3106240628106240629TC25GENIChomozygous136782898
3106240631106240632TC26GENIChomozygous136782899
3106240819106240820AG50GENIChomozygous141524562
3106242289106242290TG45GENIChomozygous141524563
3106242434106242435CT41GENIChomozygous141524564
3106242747106242748CT43GENIChomozygous141524565
3106243736106243737AG41GENIChomozygous141524566
3106240649106240650CA25GENIChomozygous144647427
3106236560106236560T25GENIChomozygous141478460
3106242821106242823GA51GENIChomozygous141478461
3106240616106240617TC25GENIChomozygous144647425
3106240619106240620TC25GENIChomozygous144647426