chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48552902185529022TG26GENIChomozygous112761768
48553002885530029TC40GENIChomozygous112761772
48553002985530030GT39GENIChomozygous119340814
48553162485531625GA18GENIChomozygous112761774
48553197185531972TC16GENIChomozygous112761776
48553577985535780GC17GENIChomozygous112761778
48553598085535981TC16GENIChomozygous112761780
48553659085536591CG29GENIChomozygous112761782
48553709285537093TC17GENIChomozygous112761784
48553868785538688TC14GENIChomozygous112761792
48553958785539588GA23GENIChomozygous112761794
48554137185541372TC29GENIChomozygous112761796
48554325985543260GA19GENIChomozygous112761800
48554416485544165CT23GENIChomozygous112761802
48554421685544217CT19GENIChomozygous112761804
48554452285544523CT17GENIChomozygous112761806
48554452785544528AG16GENIChomozygous112761808
48554461485544615GA29GENIChomozygous112761810
48554470785544708TG16GENIChomozygous112761812
48554546685545467TC15GENIChomozygous112761818
48554653285546533CT29GENICpossibly homozygous112761836
48554657785546578CT21GENIChomozygous112761838
48554693485546935TC26GENIChomozygous112761840
48554805385548054AT40GENIChomozygous112761842
48554897385548974GA11GENIChomozygous112761844
48554688385546884CG24GENIChomozygous113357402
48554753285547533CT24GENIChomozygous113357404
48554256385542564CT27GENIChomozygous113357400