chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208769664208769665TC20GENIChomozygous57066957
4208770232208770233A-14GENIChomozygous57066958
4208770260208770261CA20GENIChomozygous57607902
4208770460208770461TA15GENIChomozygous57607904
4208770921208770922CCA21GENIChomozygous57607906
4208773613208773614AG2GENICheterozygous57607908
4208774071208774072GT20GENIChomozygous57607910
4208774448208774449TC31GENIChomozygous57607912
4208775104208775105GA28GENIChomozygous57607914
4208775145208775146AG27GENIChomozygous57607916
4208776680208776681CT8GENIChomozygous57607918
4208777824208777825TC28GENIChomozygous57066962
4208779028208779029CT16GENIChomozygous57066963
4208779043208779044CG18GENIChomozygous57066964
4208779477208779485TTTTTTTT--------9GENICheterozygous57607920
4208779776208779779AAC---16GENIChomozygous57066965
4208779797208779798CCT13GENICheterozygous57607922
4208780591208780592CCAT21GENICheterozygous57607924
4208780595208780596CCACACAG23GENIChomozygous57066966
4208780595208780596CG24GENICheterozygous57607926
4208780682208780683AAT17GENICpossibly homozygous57066967
4208782951208782952CT25GENIChomozygous57066969
4208783088208783089GT27GENIChomozygous57066970
4208783142208783143AT21GENIChomozygous57607928
4208783383208783384CG20GENIChomozygous57607930
4208783620208783621GT24GENIChomozygous57066972
4208784079208784080GC36GENIChomozygous57066973
4208784088208784089GC35GENIChomozygous57066974