chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
201088455710884558CA24GENIChomozygous109422515
201088485710884858AC8GENIChomozygous109606065
201088517410885175GC19GENIChomozygous124636918
201088708510887086TC12GENIChomozygous109091586
201088731810887319AG13GENIChomozygous109392595
201088782510887826AC14GENIChomozygous109091588
201089599510895996GA12GENIChomozygous124636942
201089721510897216TC12GENIChomozygous109091594
201089730310897304TC14GENIChomozygous109091596
201089757110897572TA7GENIChomozygous109238411
201089077410890775CT15GENIChomozygous109238408
201089768810897689TA23GENIChomozygous109091598
201089807310898074GC17GENIChomozygous109091600
201089835310898354TA4GENIChomozygous109371946
201089852610898527GA16GENIChomozygous109422517
201090099010900991CT8GENIChomozygous109422519
201090111610901117GA17GENIChomozygous109422521
201090168810901689TC6GENIChomozygous109422523
201090446510904466AT5GENICheterozygous109606067
201090702010907021CT4GENIChomozygous109091610
201090952210909523GA17GENIChomozygous109091616
201090976210909763TG6GENIChomozygous109091618
201090976610909767TC8GENIChomozygous109091620
201091046410910465CA9GENIChomozygous109238415
201091047410910475AG5GENIChomozygous109392598
201091057010910571CT8GENIChomozygous109576317
201091060410910605CT12GENIChomozygous109091622
201091068410910685GA16GENIChomozygous109091624
201091098610910987CT13GENIChomozygous109422525
201091160410911605AG9GENIChomozygous109422527
201091162110911622TC11GENIChomozygous109422529
201091047510910476TC5GENIChomozygous109595347