chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52957390229573903TC9GENIChomozygous876769038
52957396529573966GA15GENIChomozygous876769039
52957405529574056AG18GENIChomozygous876769040
52957410829574109TC14GENIChomozygous876769041
52957425929574260GA15GENIChomozygous876769042
52957427529574276GT16GENIChomozygous876769043
52957469929574700GA23GENIChomozygous876769044
52957492929574930GA4GENIChomozygous876769045
52957493429574935CG5GENIChomozygous876769046
52957498329574984AG24GENIChomozygous876769047
52957520929575210GA10GENIChomozygous876769048
52957591129575912TC31GENIChomozygous876769049
52957686929576870CT6GENIChomozygous876769050
52957746929577470TC20GENIChomozygous876769051
52957757129577572TG6GENIChomozygous876769052
52957757229577573TC6GENIChomozygous876769053
52957781129577812GC26GENIChomozygous876769054
52957787729577878GA17GENIChomozygous876769055
52957827129578272TC29GENIChomozygous876769056
52957925329579254CT18GENIChomozygous876769057
52957994729579948CT14GENIChomozygous876769058
52958011629580117GA24GENIChomozygous876769059
52958176129581762CT15GENIChomozygous876769060
52958243829582439AG34GENIChomozygous876769061
52958416029584161GA14GENICheterozygous876769062
52958421929584220TG3GENICheterozygous876769063
52958596529585966CT13GENIChomozygous876769064
52958672029586721CT26GENIChomozygous876769065
52959415629594157TC4GENIChomozygous876769066
52959617029596171GT25GENIChomozygous876769067
52959867629598677AG27GENIChomozygous876769068