chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117623878117623879AT12GENIChomozygous117059152
8117625143117625144CT14GENIChomozygous117059154
8117628346117628347TC20GENIChomozygous116672088
8117628977117628978GA8GENIChomozygous117059156
8117629018117629019GA8GENIChomozygous117059158
8117632312117632313CA11GENIChomozygous117059160
8117632634117632635AG18GENICpossibly homozygous117059162
8117635278117635279CT5GENIChomozygous126674993
8117635452117635453AT8GENIChomozygous126674995
8117635649117635650CG17GENIChomozygous126674996
8117636502117636503TC11GENICheterozygous116672098
8117636978117636979CT18GENIChomozygous117059164
8117639104117639105TC14GENIChomozygous116672102
8117639162117639163TC19GENIChomozygous116672104
8117639238117639239TC22GENIChomozygous117059166
8117640819117640820GT17GENIChomozygous117059168
8117640953117640954TC5GENIChomozygous116672114
8117641100117641101AG4GENIChomozygous116672116
8117641621117641622AT12GENIChomozygous117059170
8117641666117641667TC7GENIChomozygous117059172
8117641820117641821AG8GENIChomozygous117059174
8117642273117642274AG12GENIChomozygous117059176
8117642352117642353GA9GENIChomozygous117059178
8117643598117643599CT5GENIChomozygous117059180
8117643665117643666TC12GENIChomozygous117059182
8117644194117644195TG4GENIChomozygous126674997
8117644770117644771TA19GENIChomozygous117059185
8117644970117644971GA10GENIChomozygous117059187
8117645244117645245CT17GENIChomozygous117059189
8117646921117646922CG9GENIChomozygous117059190
8117647680117647681AG14GENIChomozygous117059192