chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101281279412812795CT34GENICpossibly homozygous51620004
101281293012812931CT31GENIChomozygous51620005
101281455112814552GC21GENIChomozygous51327895
101281465812814659AAG34GENIChomozygous51620006
101281517012815171A-26GENIChomozygous51620007
101281611612816117AG15GENIChomozygous51620010
101281547412815475GGGTGTGTGTGTGTGTGTGT4GENICheterozygous52356073
101281608312816084TTGTGTGTGAGA12GENIChomozygous53131625