chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142214289822142899GT14GENIChomozygous113581458
142214365122143652AG29GENIChomozygous113581459
142214385422143855GA16GENIChomozygous113382467
142214393222143933GA13GENIChomozygous113382469
142214431022144311CA16GENIChomozygous113581460
142214466122144662GA24GENIChomozygous113581461
142214480722144808CG15GENIChomozygous113382473
142214520322145204TA8GENIChomozygous113581462
142214551122145512CA3GENIChomozygous113581463
142214688322146884CG19GENICheterozygous113382475
142214710622147107GA13GENIChomozygous113581464
142214719022147191TC15GENIChomozygous113382477
142214731722147318CT18GENIChomozygous113581465
142214734122147342GA20GENICheterozygous113581466
142214848422148485CT18GENIChomozygous113581467
142214870622148707GA16GENIChomozygous113784694
142214989022149891TC15GENIChomozygous113382485
142215176522151766TA8GENIChomozygous113382487
142215161422151615CG17GENIChomozygous118683095
142215162322151624CA19GENIChomozygous118683096
142215223522152236AG10GENIChomozygous113382489
142215285022152851CT3GENIChomozygous113581468