chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135555735135555736TC34GENIChomozygous114018179
5135555896135555898CC16GENICpossibly homozygous128242468
5135555971135555972AG13GENIChomozygous114018180
5135555981135555982AT15GENIChomozygous114018181
5135556391135556392GC24GENIChomozygous114018182
5135557381135557382TC17GENIChomozygous114018183
5135557595135557596TA20GENIChomozygous114018184
5135558239135558240AC15GENIChomozygous114018187
5135558241135558242GC16GENIChomozygous114018188
5135558617135558618CT14GENIChomozygous114018190
5135558957135558958GT18GENIChomozygous114018191
5135559336135559337CT20GENIChomozygous114018192
5135559641135559642CT16GENIChomozygous114018193
5135559766135559767GA11GENIChomozygous114018194
5135559781135559781GAG11GENIChomozygous131650154
5135559803135559803GG9GENIChomozygous131650155
5135559814135559815AG7GENIChomozygous114018195
5135560377135560378TC18GENIChomozygous114018199
5135560698135560699TA21GENIChomozygous114018200
5135560701135560702CT21GENIChomozygous114018201
5135559561135559562GA12GENIChomozygous114144586
5135559563135559564GA12GENIChomozygous114144587