chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175446141175446142TG33GENIChomozygous112961305
4175446150175446151TG23GENIChomozygous112961307
4175446152175446153CG22GENIChomozygous112961309
4175446155175446156TG22GENIChomozygous112961311
4175446158175446159TG23GENIChomozygous112961313
4175446164175446165AG25GENIChomozygous112961315
4175446175175446176GT21GENIChomozygous112961317
4175446176175446177CT21GENIChomozygous112961319
4175452838175452839AG35GENICheterozygous113222261
4175456700175456701CA4GENIChomozygous113068346
4175465176175465177TA4GENIChomozygous112961358
4175485002175485003TA16GENIChomozygous112961414
4175485049175485050GA18GENIChomozygous112961416
4175500432175500433TG22GENIChomozygous112961438
4175506052175506053TC24GENIChomozygous112961446
4175518738175518739TG10GENIChomozygous112961573
4175518750175518751TA8GENIChomozygous112961575
4175549678175549679TA55GENICheterozygous112961601
4175550112175550113TA46GENICheterozygous113406837
4175558390175558391TC10GENICheterozygous113477785
4175567208175567209TG7GENIChomozygous112961605
4175573780175573781CT22GENICheterozygous112961607
4175582856175582857CT13GENIChomozygous112961609
4175629957175629958AG189GENICheterozygous113477787
4175629964175629965TC183GENICheterozygous112961617
4175646586175646587GC25GENICheterozygous112961625
4175652665175652666GT31GENIChomozygous112961627
4175657816175657817TA19GENICpossibly homozygous112961631
4175658795175658796TC16GENICheterozygous113068364
4175658809175658810GT17GENICheterozygous113068365
4175658811175658812GA17GENICheterozygous113068366
4175658847175658848TA19GENICheterozygous112961633
4175658849175658850GA19GENICheterozygous112961635
4175658866175658867CT19GENICheterozygous112961637
4175658889175658890TA22GENICheterozygous112961639
4175658896175658897CA22GENICheterozygous113068367
4175658970175658971CT15GENICheterozygous112961647
4175682653175682654CT16GENIChomozygous112961653