chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108812005688120057G-17GENIChomozygous52573660
108812020988120210CT17GENICpossibly homozygous52573663
108812104288121043AACAGGGTTTCTCTTGTAG2GENIChomozygous52205791
108812119688121197TC9GENICheterozygous52205795
108812244188122442AG12GENICheterozygous52205807
108812263588122636CT17GENICpossibly homozygous52573666
108812270788122711TACA----2GENIChomozygous52205809
108812310788123108AG18GENICpossibly homozygous52205815
108812326888123269TC18GENICpossibly homozygous52205817
108812337788123378CG2GENIChomozygous52205823
108812640388126404TC3GENIChomozygous52205839
108812651588126516AG12GENIChomozygous52205845
108812692688126927CG5GENICheterozygous52205851
108812734188127342GA22GENICpossibly homozygous52573669
108812801988128020AT3GENICheterozygous52205853
108812885088128851CT15GENIChomozygous52573672
108812886888128869CT8GENIChomozygous52573675
108812887188128872CT10GENIChomozygous52573678
108813011888130119CA12GENIChomozygous52573681
108813025788130258AT22GENIChomozygous52573684
108813036488130365CT25GENIChomozygous52573687
108813069788130698TG11GENICpossibly homozygous52573690
108813088288130883GA9GENIChomozygous52205861