chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48552898785528988CT21GENIChomozygous112761766
48552902185529022TG24GENIChomozygous112761768
48553002885530029TC25GENIChomozygous112761772
48553162485531625GA22GENIChomozygous112761774
48553197185531972TC16GENIChomozygous112761776
48553577985535780GC12GENIChomozygous112761778
48553598085535981TC30GENIChomozygous112761780
48553659085536591CG26GENIChomozygous112761782
48553709285537093TC21GENIChomozygous112761784
48553810885538109CG21GENIChomozygous112761786
48553831385538314CT19GENIChomozygous112761788
48553860185538602CT12GENIChomozygous112761790
48553868785538688TC13GENIChomozygous112761792
48553920585539206GC16GENIChomozygous119278820
48553958785539588GA21GENIChomozygous112761794
48554137185541372TC25GENIChomozygous112761796
48554164685541647CT20GENIChomozygous112761798
48554325985543260GA26GENIChomozygous112761800
48554416485544165CT19GENIChomozygous112761802
48554421685544217CT13GENIChomozygous112761804
48554452285544523CT28GENIChomozygous112761806
48554452785544528AG28GENIChomozygous112761808
48554461485544615GA31GENIChomozygous112761810
48554470785544708TG24GENIChomozygous112761812
48554546685545467TC17GENIChomozygous112761818
48554653285546533CT32GENIChomozygous112761836
48554657785546578CT19GENIChomozygous112761838
48554693485546935TC11GENIChomozygous112761840
48554805385548054AT28GENIChomozygous112761842