chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106380553763805537T46GENIChomozygous128824310
106380554163805542C47GENIChomozygous128824311
106380554463805545T47GENIChomozygous128824312
106380555463805556GC52GENIChomozygous128824313
106380556263805563AC47GENIChomozygous116616514
106380558263805583CA47GENICpossibly homozygous116616516
106380620363806204GA57GENIChomozygous116940715
106380697763806978TC20GENIChomozygous116616518
106380733963807340CA50GENICpossibly homozygous116940717
106380836963808370AT63GENIChomozygous116616520
106380977063809771GA57GENICpossibly homozygous116940719
106381136063811360T55GENICpossibly homozygous128824315
106381382663813827CT41GENIChomozygous116940721
106381402263814025CCC18GENIChomozygous128824316
106381708563817086CT59GENIChomozygous116940723
106380933563809336AG60GENICheterozygous117296028
106380934463809345AG58GENICheterozygous117391580
106381395863813959TA21GENIChomozygous116791587