chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107227392272273923TC26GENIChomozygous116632341
107227414372274144AG20GENIChomozygous116632343
107227421472274215CT24GENIChomozygous116632345
107227446072274461TC15GENIChomozygous116632347
107227551472275515CT19GENIChomozygous117223878
107227638772276388TC28GENICheterozygous118000916
107227755972277560CG15GENIChomozygous116632349
107227780472277805CT21GENIChomozygous116632353
107227869172278692GA20GENIChomozygous116632357
107227878172278782CT21GENIChomozygous116632359
107227882072278821CG23GENIChomozygous117223880
107227947572279476CT22GENIChomozygous117223882
107227964072279641TG22GENICpossibly homozygous117223884
107227964272279643CT22GENICpossibly homozygous117223886
107227964472279645GA23GENICpossibly homozygous117223888
107227990872279909GC28GENIChomozygous116632361