chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153926342153926343GA15GENICpossibly homozygous57522071
4153926418153926419AG21GENICpossibly homozygous57522073
4153927448153927449GC23GENICpossibly homozygous57522075
4153928180153928181GGTAA1GENIChomozygous56989535
4153929077153929078CT18GENICheterozygous57522079
4153929406153929407CT17GENICpossibly homozygous57522081
4153929686153929687GA25GENIChomozygous57522083
4153931132153931133CT6GENIChomozygous57522087
4153932133153932134TTATGCCA8GENICpossibly homozygous57522089
4153932761153932762CT5GENIChomozygous56989541
4153936462153936463A-1GENIChomozygous56989542
4153936675153936676AG22GENIChomozygous57522091
4153936887153936888CG25GENIChomozygous56989543
4153937840153937841AC18GENIChomozygous57522093
4153937868153937869AG17GENIChomozygous57522095
4153938083153938084TG14GENIChomozygous56989544
4153938130153938131GA12GENICpossibly homozygous57522097
4153938700153938701GA10GENIChomozygous57522099
4153939376153939377GA19GENIChomozygous57522101
4153940057153940058GT6GENICheterozygous57522103
4153940101153940102CT9GENICpossibly homozygous57522105
4153940192153940193AG33GENIChomozygous57522107
4153940532153940533GA17GENIChomozygous57522109
4153940598153940599AAT4GENIChomozygous57522111
4153941200153941204AAGA----4GENIChomozygous57522113
4153936452153936453CT3GENIChomozygous58286985
4153936453153936454TC3GENIChomozygous58286987