chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2178355262178355263AG9GENIChomozygous111144734
2178355805178355806GA23GENICpossibly homozygous111144735
2178355947178355948TC15GENIChomozygous111144736
2178356744178356745TC12GENIChomozygous111144738
2178357130178357131AG10GENIChomozygous111144739
2178357153178357154AG4GENIChomozygous110147773
2178357249178357250TG14GENIChomozygous111144741
2178357826178357827TC25GENIChomozygous111144743
2178358259178358260GC21GENIChomozygous111144744
2178358326178358327CT18GENIChomozygous111144745
2178358346178358347GT16GENIChomozygous111144746
2178358423178358424GA18GENIChomozygous111144747
2178358525178358526CT6GENIChomozygous111144748
2178358532178358533GT5GENIChomozygous111144749
2178358578178358579CT11GENIChomozygous111144750
2178359300178359301TC17GENIChomozygous111144753
2178359904178359905TC20GENIChomozygous111144754
2178360925178360926TC6GENIChomozygous110147777
2178363580178363581AT10GENIChomozygous111144758
2178364378178364379CT23GENIChomozygous110147779
2178364491178364492GA11GENIChomozygous111144759
2178364719178364720GA14GENIChomozygous111144760
2178365044178365045AC4GENIChomozygous111144761
2178365050178365051AG7GENIChomozygous111144762
2178365182178365183GT7GENIChomozygous111144763
2178366197178366198AC5GENIChomozygous111144764
2178366273178366274TC18GENIChomozygous110798414
2178366289178366290CT17GENIChomozygous111144766