chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109014071590140716TC15GENIChomozygous116904303
109014114790141148CA30GENIChomozygous116904305
109014294090142941GA13GENIChomozygous116904307
109014342290143423GA20GENIChomozygous116904309
109014426590144266AG18GENIChomozygous116904311
109014547490145475CT29GENIChomozygous116904313
109014581890145819CT22GENIChomozygous116904315
109014837590148376TG24GENIChomozygous116904317
109014858090148581CT22GENIChomozygous116904319
109015247390152474TC2GENIChomozygous116675868
109015259890152599TC11GENIChomozygous116904321
109015259990152600TC11GENIChomozygous116904323
109015287390152874CA16GENIChomozygous116675870
109015427790154278CT12GENICpossibly homozygous116904325
109015544890155449AG27GENIChomozygous116904327
109015942190159422CA7GENIChomozygous116675874
109016058990160590TC30GENIChomozygous116904329
109016572090165721TA20GENIChomozygous116904331
109016852590168526CT20GENIChomozygous116904333