chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109099086390990864AG11GENIChomozygous116905141
109099099490990995CG10GENIChomozygous116905143
109099118590991186TC8GENIChomozygous116905147
109099118990991190CA7GENIChomozygous116905149
109099119090991191AG7GENIChomozygous116905151
109099145590991456TC10GENIChomozygous116905153
109099155590991556CG11GENIChomozygous116905155
109099174390991744TA6GENIChomozygous116905157
109099213990992140TC11GENIChomozygous116821482
109099215190992152AC9GENIChomozygous116905159
109099230490992305GC13GENIChomozygous116905161
109099316990993170GA19GENIChomozygous116905163
109099333690993337AG13GENIChomozygous116905165
109099360690993607CG14GENIChomozygous116905167
109099392190993922GA15GENIChomozygous117020578
109099396990993970GA14GENIChomozygous117088049
109099418490994185GA16GENIChomozygous116905169
109099572390995724AG17GENIChomozygous116821490
109099582790995828TC10GENIChomozygous116821492
109099627490996275CT7GENIChomozygous117088051
109099630690996307CT6GENIChomozygous117088053
109099655490996555GA8GENIChomozygous117088055
109099656190996562CT7GENIChomozygous117088057
109099659190996592GA8GENIChomozygous117088059
109099675390996754TC16GENIChomozygous116821494
109099685290996853AG14GENIChomozygous117088061
109099742490997425AG9GENIChomozygous116821496
109099775390997754GA12GENIChomozygous117088063
109099798490997985GA5GENIChomozygous117088065
109099800990998010AC4GENIChomozygous116905173
109099824390998244AG9GENIChomozygous116821498
109099826390998264CT6GENIChomozygous116821500
109099838690998387CA12GENIChomozygous117088067
109099842490998425CT11GENIChomozygous116821504
109099844790998448CT10GENIChomozygous116821505
109099848790998488CT19GENIChomozygous117088069
109099875390998754TA16GENIChomozygous116905177
109099887990998880CT10GENIChomozygous116821507
109099923190999232AG4GENIChomozygous116821509