chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104926095949260960GA20GENIChomozygous117129725
104926173549261736CT27GENIChomozygous117129727
104926189049261891CT29GENIChomozygous117129729
104926203849262039AG30GENIChomozygous116882244
104926215549262156AG29GENIChomozygous116882246
104926218249262183AG34GENIChomozygous117129731
104926258149262582TG15GENIChomozygous117129733
104926259049262591GC16GENIChomozygous117129735
104926293249262933GA25GENIChomozygous117129737
104926393149263932GA19GENICpossibly homozygous117129739
104926399949264000TC15GENIChomozygous117129741
104926430249264303TC24GENIChomozygous116882248
104926454449264545CT22GENIChomozygous117129743
104926481149264812GA16GENIChomozygous117129745
104926482049264821TA16GENIChomozygous117129747
104926483049264831TG14GENIChomozygous116588720
104926913449269135TA10GENIChomozygous116588734
104926914249269143TC8GENIChomozygous117151008
104926951849269519CA25GENIChomozygous117129749
104926958249269583AG33GENIChomozygous117129751
104927013349270134CT44GENIChomozygous117151009
104927336649273367AG12GENIChomozygous116882258
104927484149274842GA15GENIChomozygous117129753
104927736649277367CT31GENIChomozygous116882280
104927831149278312GT31GENIChomozygous117129755
104927933649279337AC28GENIChomozygous116882286
104927988049279881AG18GENIChomozygous117129757
104928146949281470GA26GENIChomozygous116882306
104928244249282443GA25GENIChomozygous117129759
104928340049283401CT22GENIChomozygous116882324
104928783649287837CT31GENIChomozygous116931997
104928804449288045CT25GENIChomozygous116882332
104928864049288641CT34GENIChomozygous117129761
104929196049291961CA27GENIChomozygous116588736
104929200649292007AT30GENIChomozygous116588738
104929200749292008TA30GENIChomozygous116588740
104929251849292519GA31GENIChomozygous117129763
104929563349295634AG43GENIChomozygous116882336