chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117623878117623879AT19GENIChomozygous117059152
8117625143117625144CT22GENIChomozygous117059154
8117628346117628347TC12GENIChomozygous116672088
8117628977117628978GA3GENIChomozygous117059156
8117629018117629019GA8GENIChomozygous117059158
8117632312117632313CA8GENIChomozygous117059160
8117632634117632635AG13GENIChomozygous117059162
8117636502117636503TC9GENIChomozygous116672098
8117636978117636979CT7GENIChomozygous117059164
8117639104117639105TC13GENIChomozygous116672102
8117639162117639163TC13GENIChomozygous116672104
8117639238117639239TC14GENIChomozygous117059166
8117640953117640954TC9GENIChomozygous116672114
8117641621117641622AT6GENIChomozygous117059170
8117641666117641667TC4GENIChomozygous117059172
8117641820117641821AG16GENIChomozygous117059174
8117642273117642274AG21GENIChomozygous117059176
8117642352117642353GA23GENIChomozygous117059178
8117643665117643666TC8GENIChomozygous117059182
8117644397117644398GA6GENIChomozygous117059184
8117644770117644771TA12GENIChomozygous117059185
8117644970117644971GA12GENIChomozygous117059187
8117645244117645245CT15GENIChomozygous117059189
8117646921117646922CG13GENIChomozygous117059190
8117647680117647681AG4GENIChomozygous117059192
8117647868117647869AG12GENIChomozygous117059194