chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3131010314131010315TTG5GENIChomozygous58477848
3131010697131010698TTA21GENICpossibly homozygous58477850
3131010763131010764TC44GENIChomozygous58477851
3131011820131011821GC23GENIChomozygous57677914
3131013352131013353TC2GENIChomozygous57677916
3131013356131013357AC3GENIChomozygous57677918
3131015291131015292GGTTATTTATTTAT3GENIChomozygous57677924
3131015451131015452TC27GENIChomozygous57677926
3131015572131015573TC33GENIChomozygous57677928
3131016350131016351AG36GENIChomozygous57677932
3131016835131016836TC22GENIChomozygous57677936
3131017390131017391AT32GENIChomozygous57677938
3131017701131017702AG22GENIChomozygous57677940
3131017787131017788GGCT11GENIChomozygous57677942
3131018010131018011T-21GENIChomozygous57677945
3131018194131018195CT30GENIChomozygous58477855
3131019069131019070AG24GENIChomozygous57677949
3131019275131019276GA23GENIChomozygous57677953
3131019341131019342GA27GENIChomozygous58477857
3131020111131020112TC34GENIChomozygous57677957
3131020203131020204CT21GENIChomozygous58477859
3131022126131022127GT21GENIChomozygous58477861
3131022283131022284C-5GENICheterozygous57677969
3131022445131022446TC23GENIChomozygous57677971
3131024795131024796GA23GENIChomozygous58477863
3131016640131016641CCTTTT3GENIChomozygous58624065
3131021123131021127TTGA----8GENIChomozygous58624066