chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14114928999114929003AATT----8GENIChomozygous48923198
14114929045114929049CCTC----6GENICheterozygous49293706
14114930159114930160CT18GENIChomozygous48923200
14114930754114930755AC19GENIChomozygous48923203
14114931772114931773TC18GENIChomozygous48923204
14114931862114931863CT20GENICpossibly homozygous48923205
14114931879114931880GA20GENICpossibly homozygous48923206
14114931973114931974TA17GENIChomozygous48923207
14114932417114932418GC11GENICpossibly homozygous48923208
14114932447114932448CT6GENIChomozygous48923209
14114932825114932826GA10GENICheterozygous48923210
14114932979114932980GA24GENICpossibly homozygous48923211
14114933187114933188CA14GENIChomozygous48923212
14114933217114933218AT5GENICheterozygous48923213
14114934473114934474AG19GENIChomozygous48923214
14114934722114934723AG16GENICpossibly homozygous48923215
14114935201114935202GA7GENICpossibly homozygous48923216
14114935887114935888TA7GENICpossibly homozygous48923217