chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
201088455710884558CA25GENIChomozygous109422515
201088782510887826AC30GENIChomozygous109091588
201088708510887086TC23GENIChomozygous109091586
201089721510897216TC22GENIChomozygous109091594
201089730310897304TC31GENIChomozygous109091596
201089768810897689TA22GENIChomozygous109091598
201089807310898074GC12GENIChomozygous109091600
201089852610898527GA21GENIChomozygous109422517
201090099010900991CT23GENIChomozygous109422519
201090111610901117GA27GENIChomozygous109422521
201090168810901689TC23GENIChomozygous109422523
201089077410890775CT23GENIChomozygous109238408
201089122110891222CA31GENICpossibly homozygous109238409
201089757110897572TA24GENIChomozygous109238411
201090702010907021CT29GENIChomozygous109091610
201090952210909523GA25GENIChomozygous109091616
201090976210909763TG19GENIChomozygous109091618
201090976610909767TC21GENIChomozygous109091620
201091068410910685GA26GENIChomozygous109091624
201091098610910987CT20GENIChomozygous109422525
201091160410911605AG20GENIChomozygous109422527
201091162110911622TC28GENIChomozygous109422529
201091212010912121GC22GENIChomozygous109422531