chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
92735813727358138CT23GENIChomozygous120390373
92736129727361298CG12GENIChomozygous117693776
92736162327361624TG33GENIChomozygous117296531
92736306227363063AG41GENIChomozygous117296547
92736355727363558GA9GENIChomozygous117296549
92736363527363636GT3GENIChomozygous117296551
92739887927398880TA23GENIChomozygous117296603
92740040327400404GC25GENIChomozygous117296608
92740106827401069AT15GENIChomozygous117296618
92740370927403710TC25GENIChomozygous117693784
92740842027408421CT29GENIChomozygous120390375
92740987827409879CT42GENIChomozygous117693790
92741316527413166GA18GENIChomozygous120333077
92741316627413167TG18GENIChomozygous117804678
92741578327415784TA18GENIChomozygous120390377