chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261801928261801929AG15GENIChomozygous120881548
1261807504261807505TA20GENIChomozygous108630051
1261808828261808829CT38GENIChomozygous120881549
1261814325261814326GA35GENIChomozygous120881550
1261815342261815343CA38GENIChomozygous109545425
1261815343261815344AC39GENIChomozygous108782642
1261815681261815682AC38GENIChomozygous108630057
1261816193261816194AT14GENIChomozygous108630058
1261817916261817917CA28GENIChomozygous108630066
1261819164261819165CA21GENIChomozygous120477211
1261823918261823919CA28GENIChomozygous120494248
1261823920261823921AG29GENIChomozygous120494249
1261823921261823922TG29GENIChomozygous120494250
1261824126261824127GT25GENIChomozygous120494251
1261824127261824128TG24GENIChomozygous120477212
1261825376261825377CT18GENIChomozygous108630083
1261825631261825632TA16GENIChomozygous108782655
1261825633261825634AT16GENIChomozygous108782656
1261832175261832176GA16GENIChomozygous108630091