chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106380448663804487CT26GENIChomozygous116616512
106380553763805537T25GENIChomozygous128824310
106380554163805542C26GENIChomozygous128824311
106380554463805545T26GENIChomozygous128824312
106380555463805556GC27GENIChomozygous128824313
106380556263805563AC29GENIChomozygous116616514
106380558263805583CA27GENIChomozygous116616516
106380697763806978TC7GENIChomozygous116616518
106380836963808370AT32GENIChomozygous116616520
106380854763808548GA24GENIChomozygous116616522
106380905963809059C19GENIChomozygous128824314
106380933563809336AG31GENICheterozygous117296028
106381100263811003GT20GENIChomozygous117998307
106381136063811360T21GENIChomozygous128824315
106381272863812729GA35GENIChomozygous116616524
106381331163813312GA13GENICpossibly homozygous116616526
106381388963813890TC17GENICpossibly homozygous116616528
106381395763813958TC11GENIChomozygous117998308
106381402263814025CCC9GENIChomozygous128824316
106381463663814640AGAC25GENIChomozygous128824317
106381489163814892CT26GENIChomozygous116616530
106381741963817426AGTTATT31GENIChomozygous128824318
106381752563817526GA29GENIChomozygous116616532
106381767563817676AC32GENIChomozygous116616534
106381813363818134TC33GENIChomozygous116616536
106380934463809345AG32GENICheterozygous117391580
106381395863813959TA11GENIChomozygous116791587