chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128743071128743072CT33GENIChomozygous116721915
8128743825128743826GA25GENIChomozygous116721916
8128744416128744417TC29GENIChomozygous116721917
8128744747128744748TC19GENIChomozygous116721918
8128744944128744945CT20GENIChomozygous116721919
8128745012128745013CT19GENICpossibly homozygous116721920
8128745018128745019TA15GENICheterozygous116721921
8128745019128745020TG16GENICheterozygous116721922
8128745177128745178GA16GENIChomozygous116721925
8128745352128745353CT34GENIChomozygous116721926
8128745430128745431AG36GENIChomozygous116721927
8128745797128745798AG31GENIChomozygous116721928
8128745837128745838CA34GENIChomozygous116721929
8128745952128745953AG30GENIChomozygous116721930
8128747675128747676CT9GENIChomozygous116721931
8128747790128747791CG16GENIChomozygous116721932
8128747915128747916CG17GENIChomozygous116721933
8128748186128748187GC21GENIChomozygous116721934
8128748240128748241TC27GENIChomozygous116721935
8128748977128748978TG13GENIChomozygous116721936
8128749284128749285GA32GENIChomozygous116721937
8128749918128749919AT37GENIChomozygous116721938
8128750856128750857AC30GENIChomozygous116721939
8128750903128750904TC32GENICheterozygous116721940
8128750911128750912CT30GENICheterozygous116721941
8128751423128751424GT20GENIChomozygous116721943
8128752231128752232CA25GENIChomozygous116721944
8128752827128752828TA33GENIChomozygous116721945
8128753421128753422GA24GENIChomozygous116721946
8128753731128753732GA19GENIChomozygous116721947
8128754010128754011AT23GENIChomozygous116721948