chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2183451324183451325TC61GENIChomozygous110160917
2183453608183453609TC46GENIChomozygous110160918
2183455226183455227TC54GENIChomozygous110160919
2183455390183455391GA44GENIChomozygous110160920
2183455789183455790CT41GENIChomozygous110160921
2183459022183459023AG38GENIChomozygous110160922
2183460753183460754CA28GENIChomozygous110160923
2183463443183463444TG41GENIChomozygous110160924
2183463588183463589GT21GENIChomozygous110160925
2183463656183463657CT55GENIChomozygous110160926
2183464275183464276TC35GENIChomozygous110160927
2183464455183464456TC38GENIChomozygous110160928
2183466760183466761GT17GENIChomozygous110160929
2183467834183467835AT43GENICpossibly homozygous110160930
2183474861183474862AC34GENICheterozygous110160931
2183476922183476923AG41GENIChomozygous110160932
2183480182183480183GA47GENIChomozygous110160933
2183480256183480257CT43GENIChomozygous110160934
2183481038183481039CT45GENIChomozygous110160935
2183483780183483781CT42GENIChomozygous110160936
2183483873183483874AG33GENIChomozygous110160937
2183483905183483906CT39GENIChomozygous110160938
2183484188183484189TG52GENIChomozygous110160939
2183484228183484229TC51GENIChomozygous110160940
2183484323183484324TC51GENIChomozygous110160941
2183484744183484745AG39GENICheterozygous110160942
2183484935183484936CT38GENIChomozygous110160943
2183485128183485129GA28GENIChomozygous110160944
2183485165183485166CT36GENIChomozygous110160945
2183485231183485232TC36GENIChomozygous110160946
2183485232183485233TC34GENIChomozygous110160947
2183485327183485328AG49GENIChomozygous110160948
2183486040183486041GA63GENICpossibly homozygous110160949
2183486836183486837TC50GENIChomozygous110160950
2183487668183487669AT36GENIChomozygous110160951