chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157382773157382774GC62GENIChomozygous112906055
4157386245157386246AT40GENICheterozygous128137664
4157388743157388744TG54GENIChomozygous112906057
4157392261157392262GA52GENIChomozygous112906067
4157396167157396168GA46GENIChomozygous112906073
4157397875157397876CT52GENIChomozygous112906075
4157399492157399493TC34GENIChomozygous112906077
4157399850157399851CA48GENIChomozygous112906079
4157400365157400366GA39GENIChomozygous112906081
4157400388157400389CA41GENIChomozygous112906083
4157400419157400420TC36GENIChomozygous112906085
4157401383157401384AG1GENIChomozygous112906087
4157401384157401385CT1GENIChomozygous112906089
4157401399157401401AT5GENIChomozygous128096107
4157386255157386256TG44GENICheterozygous113062872
4157386262157386263TA45GENICheterozygous113062874
4157386275157386276G53GENICheterozygous128096103
4157393200157393200TC35GENICpossibly homozygous128096104
4157398568157398568T41GENICpossibly homozygous128096105
4157401391157401391GC2GENIChomozygous128096106
4157402357157402358AG46GENICpossibly homozygous112906093
4157403131157403132TA48GENIChomozygous112906095
4157403947157403948TC45GENIChomozygous112906097
4157404786157404787CG51GENIChomozygous112906099
4157405666157405667GA53GENIChomozygous112906101
4157406195157406196G42GENIChomozygous128096111
4157401431157401431AA13GENIChomozygous128096108
4157401433157401433ATACATACACACAAATACACACATATACACACATAT13GENIChomozygous128096109
4157402468157402469G45GENIChomozygous128096110
4157406949157407070GAGTTCTACCTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC13GENICheterozygous128096112
4157407511157407512AC47GENIChomozygous112906103
4157407579157407579A34GENIChomozygous128096113
4157407709157407710CT39GENIChomozygous112906105
4157408171157408172CT42GENICpossibly homozygous112906107