chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128742239128742240GA55GENIChomozygous116901713
8128742240128742241AG55GENIChomozygous116901715
8128744944128744945CT44GENIChomozygous116721919
8128743071128743072CT43GENIChomozygous116721915
8128743825128743826GA42GENIChomozygous116721916
8128744416128744417TC37GENIChomozygous116721917
8128744747128744748TC46GENIChomozygous116721918
8128743691128743691A38GENIChomozygous128647222
8128744053128744053A52GENIChomozygous128647223
8128745177128745178GA44GENIChomozygous116721925
8128745352128745353CT41GENIChomozygous116721926
8128747675128747676CT25GENIChomozygous116721931
8128745430128745431AG28GENIChomozygous116721927
8128745797128745798AG58GENIChomozygous116721928
8128745837128745838CA58GENICpossibly homozygous116721929
8128745952128745953AG53GENIChomozygous116721930
8128747723128747729CCCTCT17GENIChomozygous128647224
8128747790128747791CG35GENIChomozygous116721932
8128747915128747916CG56GENIChomozygous116721933
8128748186128748187GC63GENIChomozygous116721934
8128748240128748241TC60GENIChomozygous116721935
8128748977128748978TG49GENIChomozygous116721936
8128749284128749285GA53GENIChomozygous116721937
8128749448128749449A47GENIChomozygous128647225
8128749918128749919AT54GENICpossibly homozygous116721938
8128750856128750857AC25GENIChomozygous116721939
8128751423128751424GT43GENIChomozygous116721943
8128752231128752232CA57GENIChomozygous116721944
8128752827128752828TA67GENIChomozygous116721945
8128753421128753422GA49GENIChomozygous116721946
8128753731128753732GA44GENIChomozygous116721947
8128754010128754011AT44GENIChomozygous116721948
8128754349128754350CT56GENICpossibly homozygous117176281
8128749816128749820ACAC49GENIChomozygous128647226
8128750904128750904CCTCTAGTACAGTACTCCTCTAGTACAGTACC30GENIChomozygous128647227