chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105972563859725639GC5INTERGENICheterozygous51466104
105972574459725745TTAA1INTERGENIChomozygous51466105
105972678459726785TC4INTERGENIChomozygous51466106
105972688759726888AG2INTERGENIChomozygous51466107
105972712259727123CT14INTERGENIChomozygous51466108
105972768859727689AG5INTERGENIChomozygous51466111
105973042059730421AC19INTERGENIChomozygous51466112
105973071559730716AT2INTERGENIChomozygous51466114
105973077359730774TC4INTERGENIChomozygous51466115
105973094559730946AG8INTERGENICpossibly homozygous51466116
105973113759731138GGAA1INTERGENIChomozygous51466117
105973117159731172GA5INTERGENIChomozygous51466119
105973295259732953GA2INTERGENIChomozygous51466122
105973473259734733TC9INTERGENICpossibly homozygous51466126
105973492359734924GT7INTERGENIChomozygous51466127
105973529359735294GA15INTERGENICheterozygous51466130
105973536159735362GGGA11INTERGENIChomozygous51466131
105973539859735399AT8INTERGENICpossibly homozygous51466132
105973539959735400AC8INTERGENICpossibly homozygous51466133
105973541959735420CCAAT11INTERGENICheterozygous51466135
105973547459735475CA3INTERGENICheterozygous51466138
105973548459735485GA1INTERGENIChomozygous51466139
105973643559736436AAT7INTERGENICheterozygous51466142
105973701759737018AC1INTERGENIChomozygous51466145