chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106226470462264705CT34GENICpossibly homozygous116613586
106226504262265043TC34GENIChomozygous116613588
106226543962265440TC53GENIChomozygous116613589
106226548562265486AG44GENIChomozygous116613591
106226927562269276GA65GENIChomozygous116613593
106226928462269285AG62GENIChomozygous116613595
106227091362270914TA43GENIChomozygous116613597
106227094762270948AG38GENIChomozygous116613599
106227151862271519AG52GENIChomozygous116613601