chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157382773157382774GC28GENIChomozygous112906055
4157388743157388744TG27GENIChomozygous112906057
4157392261157392262GA19GENIChomozygous112906067
4157393200157393200TC16GENICpossibly homozygous128096104
4157396167157396168GA19GENIChomozygous112906073
4157397875157397876CT35GENIChomozygous112906075
4157398568157398568T18GENICpossibly homozygous128096105
4157399492157399493TC19GENIChomozygous112906077
4157399850157399851CA18GENIChomozygous112906079
4157400365157400366GA33GENIChomozygous112906081
4157400388157400389CA27GENIChomozygous112906083
4157400419157400420TC26GENIChomozygous112906085
4157401383157401384AG1GENIChomozygous112906087
4157401384157401385CT1GENIChomozygous112906089
4157401391157401391GC1GENIChomozygous128096106
4157401399157401401AT2GENIChomozygous128096107
4157401431157401431AA5GENIChomozygous128096108
4157401433157401433ATACATACACACAAATACACACATATACACACATAT5GENIChomozygous128096109
4157402357157402358AG25GENIChomozygous112906093
4157402468157402469G15GENIChomozygous128096110
4157403131157403132TA15GENIChomozygous112906095
4157403947157403948TC20GENIChomozygous112906097
4157404786157404787CG24GENIChomozygous112906099
4157405666157405667GA19GENIChomozygous112906101
4157406195157406196G35GENIChomozygous128096111
4157406949157407070GAGTTCTACCTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC4GENICheterozygous128096112
4157407511157407512AC22GENIChomozygous112906103
4157407579157407579A24GENIChomozygous128096113
4157407709157407710CT17GENIChomozygous112906105
4157408171157408172CT23GENIChomozygous112906107