chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184483368744833688CG19GENIChomozygous110331139
184485442144854422TG18GENIChomozygous110331143
184486039044860391AG34GENICheterozygous119491304
184486041244860413CT35GENICheterozygous119491306
184486103844861039CT77GENICheterozygous119527496
184486104844861049GA74GENICheterozygous119527498
184486105444861055GT78GENICheterozygous119546079
184486106444861065GC65GENICheterozygous119546081
184486124244861243CT50GENICheterozygous119527502
184486377444863775TA35GENICheterozygous119546082
184486377544863776GA36GENICheterozygous119546084
184486378044863781TA35GENICheterozygous119546086
184486378744863788AC40GENICheterozygous119546087
184486380344863804GT49GENICheterozygous119546089
184486382144863822TG53GENICheterozygous119546090
184486384344863844GT47GENICheterozygous119546092
184486384844863849GT47GENICheterozygous119546094
184486677744866778CG18GENIChomozygous110331145
184487230744872308AG22GENIChomozygous110331147
184488742944887430CT27GENIChomozygous110331149