chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109014071590140716TC39GENIChomozygous116904303
109014114790141148CA32GENIChomozygous116904305
109014294090142941GA32GENIChomozygous116904307
109014342290143423GA43GENIChomozygous116904309
109014426590144266AG38GENIChomozygous116904311
109014547490145475CT33GENIChomozygous116904313
109014581890145819CT33GENIChomozygous116904315
109014837590148376TG30GENIChomozygous116904317
109014858090148581CT29GENIChomozygous116904319
109015237990152380TC6GENIChomozygous117068517
109015427790154278CT36GENIChomozygous116904325
109015544890155449AG26GENIChomozygous116904327
109016058990160590TC32GENIChomozygous116904329
109016572090165721TA31GENIChomozygous116904331
109016852590168526CT33GENIChomozygous116904333
109015123790151238GC31GENIChomozygous116675866
109015247390152474TC13GENIChomozygous116675868
109015287390152874CA26GENIChomozygous116675870