chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117623878117623879AT27GENIChomozygous117059152
8117625143117625144CT24GENIChomozygous117059154
8117628346117628347TC37GENIChomozygous116672088
8117628977117628978GA44GENIChomozygous117059156
8117629018117629019GA40GENIChomozygous117059158
8117632312117632313CA22GENIChomozygous117059160
8117632634117632635AG29GENIChomozygous117059162
8117636502117636503TC21GENIChomozygous116672098
8117636978117636979CT33GENIChomozygous117059164
8117639104117639105TC28GENIChomozygous116672102
8117639162117639163TC37GENIChomozygous116672104
8117639238117639239TC32GENIChomozygous117059166
8117640819117640820GT25GENIChomozygous117059168
8117640953117640954TC31GENIChomozygous116672114
8117641100117641101AG36GENIChomozygous116672116
8117641621117641622AT41GENIChomozygous117059170
8117641666117641667TC38GENIChomozygous117059172
8117641820117641821AG19GENIChomozygous117059174
8117642273117642274AG24GENIChomozygous117059176
8117642352117642353GA23GENIChomozygous117059178
8117643598117643599CT20GENIChomozygous117059180
8117643665117643666TC26GENIChomozygous117059182
8117644397117644398GA28GENIChomozygous117059184
8117644970117644971GA17GENIChomozygous117059187
8117645244117645245CT32GENIChomozygous117059189
8117645709117645710CT2GENIChomozygous116672128
8117646921117646922CG23GENIChomozygous117059190
8117647680117647681AG23GENIChomozygous117059192
8117647868117647869AG26GENIChomozygous117059194