chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76145300861453009TC65GENIChomozygous53931898
76145332061453322TC--18GENICheterozygous53931899
76145333661453338TC--22GENICheterozygous54196246
76145389361453894AG50GENICpossibly homozygous53931901
76145389761453898AG48GENICpossibly homozygous53931902
76145599461455995CA36GENICheterozygous53931903
76145631561456316AT46GENIChomozygous53931904
76145696261456963TC53GENIChomozygous53931905
76145721961457220AC82GENIChomozygous53931906
76145743561457436TC64GENIChomozygous53931907
76145749261457493TA82GENICpossibly homozygous53931908
76145757761457578TA73GENIChomozygous53931909
76145810361458104CA65GENIChomozygous53931910
76145826961458279TGTGTGTGTA----------19GENIChomozygous53931911
76145833961458341TG--8GENICpossibly homozygous53931912
76145865361458654GGA57GENIChomozygous53931913
76145947961459481TG--21GENIChomozygous53931914
76145950861459510AT--29GENICpossibly homozygous53931915
76146244561462446AG45GENIChomozygous53931916
76146255261462553AC79GENIChomozygous53931917
76146331561463316AG45GENIChomozygous53931918
76146335061463351GA45GENIChomozygous53931919
76146433261464333G-36GENICpossibly homozygous53931920
76146479561464796TC62GENICpossibly homozygous53931921
76146489061464891TG45GENIChomozygous53931922
76146489161464892TG46GENIChomozygous53931923
76146496261464963AG67GENIChomozygous53931924
76146499861464999TC70GENIChomozygous53931925
76146533361465334AG42GENIChomozygous53931926
76146573161465732GC49GENIChomozygous53931927
76146574261465746AAAT----40GENIChomozygous53931928
76146582761465828TC62GENIChomozygous53931929
76146602461466025GC51GENIChomozygous53931930
76146652161466522CT38GENICpossibly homozygous53931931
76146664161466642A-8GENICpossibly homozygous53931932
76146682761466828AATGACTACAC14GENIChomozygous53931933