chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135828470135828471TG6GENIChomozygous54741114
6135829593135829594AG32GENIChomozygous54741116
6135829792135829793AAG11GENICpossibly homozygous54741118
6135830217135830218TG6GENIChomozygous54741120
6135830267135830268CCTTTTTTTTTTTTTTT3GENIChomozygous55542272
6135830287135830288AG5GENIChomozygous54741122
6135830505135830506GT17GENIChomozygous54741124
6135831064135831065CCTT13GENIChomozygous54741126
6135832547135832548AG30GENIChomozygous54741128
6135832840135832842GT--11GENIChomozygous54741134
6135833113135833114CT25GENIChomozygous54741136
6135833610135833611T-12GENICheterozygous55542274
6135835541135835542TC31GENIChomozygous54741138
6135837068135837070AC--6GENICheterozygous54741140
6135837071135837075CACT----7GENICheterozygous55542277
6135837578135837579A-12GENIChomozygous54741142
6135838144135838145CCT7GENIChomozygous55542279
6135838647135838648AG31GENIChomozygous54741144
6135838907135838908CT35GENICpossibly homozygous54741146
6135839555135839556CT47GENIChomozygous54741148