chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117623878117623879AT20GENIChomozygous117059152
8117625143117625144CT24GENIChomozygous117059154
8117625282117625290TTCTTTCT17GENIChomozygous128635905
8117626908117626908GG26GENIChomozygous132125049
8117632634117632635AG17GENIChomozygous117059162
8117628346117628347TC20GENIChomozygous116672088
8117628977117628978GA20GENIChomozygous117059156
8117629018117629019GA24GENIChomozygous117059158
8117632312117632313CA19GENICpossibly homozygous117059160
8117634319117634320GT19GENICpossibly homozygous116672094
8117634746117634756TGTGTGTGAG9GENIChomozygous132322576
8117634899117634913GTGTGTGTGAGAGT16GENIChomozygous132322577
8117636502117636503TC33GENIChomozygous116672098
8117636978117636979CT23GENIChomozygous117059164
8117637700117637700CA20GENIChomozygous128635907
8117639104117639105TC22GENIChomozygous116672102
8117639162117639163TC25GENIChomozygous116672104
8117639238117639239TC36GENIChomozygous117059166
8117640351117640352C27GENIChomozygous128635908
8117640819117640820GT32GENIChomozygous117059168
8117640953117640954TC32GENIChomozygous116672114
8117641100117641101AG24GENIChomozygous116672116
8117641621117641622AT24GENIChomozygous117059170
8117641666117641667TC27GENIChomozygous117059172
8117641820117641821AG19GENIChomozygous117059174
8117641993117641993CA27GENIChomozygous132125050
8117642273117642274AG31GENIChomozygous117059176
8117642352117642353GA34GENIChomozygous117059178
8117643598117643599CT13GENIChomozygous117059180
8117643665117643666TC16GENIChomozygous117059182
8117644397117644398GA22GENIChomozygous117059184
8117644770117644771TA21GENIChomozygous117059185
8117644970117644971GA28GENIChomozygous117059187
8117645244117645245CT25GENIChomozygous117059189
8117646921117646922CG21GENIChomozygous117059190
8117647211117647212G22GENIChomozygous131694504
8117647680117647681AG24GENIChomozygous117059192
8117647868117647869AG21GENIChomozygous117059194