chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109043504490435045TA7GENIChomozygous52206531
109043682990436830AG18GENIChomozygous51538456
109043708590437086AAT21GENIChomozygous52206533
109043770490437705TTA19GENICpossibly homozygous51538457
109043744090437441GA13GENIChomozygous51736655
109043826890438269C-12GENIChomozygous51736657
109043851690438517GT18GENIChomozygous51736659
109044062690440627TA32GENIChomozygous51538459
109044074190440742A-20GENIChomozygous52206535
109044120590441206GA17GENIChomozygous51736661
109044202490442025TC19GENIChomozygous51538461
109044274390442744T-15GENIChomozygous51538462
109044292790442928CG24GENIChomozygous51538463
109044404690444047AG14GENIChomozygous51736663
109044505290445053TC17GENIChomozygous51538467
109044523390445234CT14GENIChomozygous51538468
109044525490445255T-15GENIChomozygous51538469
109044546390445464CCAAA4GENICheterozygous51538471
109044546390445464CCAAAA4GENICheterozygous52445639
109044162090441634CACACACACACACA--------------6GENICheterozygous52445633
109044162290441634CACACACACACA------------6GENICheterozygous52445635
109044554390445544CG12GENIChomozygous51538472
109044601090446011AT23GENIChomozygous51538473
109044629890446299GT20GENIChomozygous51538474
109044700090447001AG28GENIChomozygous51538475
109044700190447002CT28GENIChomozygous51538476