chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905051249050520TTTTTTTA--------12GENIChomozygous50455731
124905052349050524AC12GENIChomozygous50230912
124905052749050528AC12GENIChomozygous50230914
124905053149050532AC14GENIChomozygous50230916
124905053549050536AC12GENIChomozygous50230918
124905175549051756GGT5GENICheterozygous50546601
124905175649051761TTTTT-----5GENICheterozygous50546602
124905205549052056C-16GENICheterozygous50546603
124905236449052365AT44GENIChomozygous50230932
124905238449052394TGAGTGTGTG----------35GENIChomozygous50491773
124905276849052769TC34GENIChomozygous50230934
124905571649055717TTG10GENICheterozygous50343654
124905572249055723TG15GENICpossibly homozygous50513695
124905614649056147CA24GENIChomozygous50230942
124905616249056163AAGCTATTTCTTACTCCCAACTTCCCCGATGGGCACCCATTACCTGTTCCCTGCTGC36GENIChomozygous50513699