chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905139449051395CA20GENICpossibly homozygous50230926
124905230049052301AAGT3GENICheterozygous50230930
124905236449052365AT10GENIChomozygous50230932
124905276849052769TC16GENIChomozygous50230934
124905539549055396AC18GENIChomozygous50230936
124905566749055668GGA2GENICheterozygous50230938
124905571649055717TTG2GENICheterozygous50343654
124905614649056147CA8GENICpossibly homozygous50230942
124905616249056163AAGCTATTTCTTACTCCCAACTTCCCCGATGGGCACCCATTACCTGTTCCCTGCTGC1GENIChomozygous50513699
124905572249055723TG2GENIChomozygous50513695
124905593049055933AAG---1GENIChomozygous50513697