chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208769135208769136TA21GENIChomozygous58487781
4208769664208769665TC17GENIChomozygous57066957
4208769787208769788TC30GENICpossibly homozygous58487782
4208770232208770233A-19GENIChomozygous57066958
4208770587208770599ACACACACACAC------------5GENIChomozygous58487783
4208771274208771275GT30GENIChomozygous58487784
4208773189208773190CT23GENIChomozygous58487785
4208773218208773219CT23GENIChomozygous58487786
4208773791208773792GA17GENIChomozygous58487787
4208774071208774072GT16GENIChomozygous57607910
4208774111208774112CT21GENIChomozygous58487788
4208774448208774449TC33GENIChomozygous57607912
4208774540208774541TA22GENIChomozygous58487789
4208775111208775112GC32GENIChomozygous58487790
4208775145208775146AG34GENIChomozygous57607916
4208777824208777825TC32GENIChomozygous57066962
4208779028208779029CT31GENIChomozygous57066963
4208779043208779044CG30GENIChomozygous57066964
4208779776208779779AAC---11GENIChomozygous57066965
4208779797208779798CCT9GENICheterozygous57607922
4208780166208780167TC21GENIChomozygous58487791
4208780385208780386TG20GENICpossibly homozygous58487792
4208780593208780594CCAT6GENICheterozygous58531211
4208780595208780596CCACACAG5GENICheterozygous57066966
4208780595208780596CCATACATACACAG5GENICheterozygous58601502
4208780682208780683AAT9GENICpossibly homozygous57066967
4208781237208781238AC31GENIChomozygous58487793
4208782213208782214CT15GENIChomozygous58487794
4208782951208782952CT19GENIChomozygous57066969
4208783383208783384CG28GENIChomozygous57607930
4208783620208783621GT16GENIChomozygous57066972
4208784079208784080GC20GENIChomozygous57066973
4208784088208784089GC21GENIChomozygous57066974
4208779797208779798CCTT9GENICheterozygous58369291