chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905051249050520TTTTTTTA--------8GENIChomozygous50455731
124905051449050515TTC15GENICheterozygous50230908
124905051549050516TTTTC15GENICheterozygous50230910
124905052349050524AC14GENIChomozygous50230912
124905052749050528AC16GENIChomozygous50230914
124905175549051756G-12GENICheterozygous50230928
124905175649051760TTTT----7GENICheterozygous50470669
124905236449052365AT48GENICpossibly homozygous50230932
124905238449052394TGAGTGTGTG----------34GENIChomozygous50491773
124905276849052769TC39GENIChomozygous50230934
124905614649056147CA13GENIChomozygous50230942
124905571649055717TTG11GENICpossibly homozygous50343654