chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261301674261301675CT27GENIChomozygous125494194
1261302616261302617CA12GENIChomozygous125443641
1261304620261304621CT16GENIChomozygous125324441
1261309263261309264GA10GENIChomozygous125443647
1261309654261309655AG5GENIChomozygous125443649
1261311279261311280TG14GENIChomozygous125324453
1261312555261312556AG14GENIChomozygous125382931
1261313649261313650GA19GENIChomozygous125443651
1261315421261315422CT24GENIChomozygous125443655
1261316340261316341GC13GENIChomozygous125443657
1261316485261316486GA17GENIChomozygous125494195
1261316956261316957CA14GENIChomozygous125324458
1261317224261317225TC15GENIChomozygous125324459
1261317440261317441CG15GENIChomozygous125494196
1261317676261317677GA9GENIChomozygous125443663
1261319680261319681CT8GENIChomozygous125494197