chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264095442264095443AG67GENICpossibly homozygous778808009
1264095886264095887AG67GENIChomozygous778808010
1264097432264097433TC42GENIChomozygous778808011
1264097633264097634AC73GENIChomozygous778808012
1264097682264097683GA58GENIChomozygous778808013
1264098597264098598CT32GENICpossibly homozygous778808014
1264098630264098631AG33GENIChomozygous778808015
1264098735264098736CT73GENICheterozygous778808016
1264099882264099883CT59GENICpossibly homozygous778808017
1264099931264099932CT62GENIChomozygous778808018
1264100059264100060TA59GENIChomozygous778808019
1264100188264100189AG54GENICpossibly homozygous778808020
1264100432264100433GA65GENICpossibly homozygous778808021
1264100637264100638TC54GENIChomozygous778808022
1264101191264101192TC36GENIChomozygous778808023
1264101219264101220CT21GENIChomozygous778808024
1264101725264101726TA48GENIChomozygous778808025
1264101841264101842AG54GENICpossibly homozygous778808026
1264102013264102014GA56GENIChomozygous778808027
1264102022264102023CT60GENIChomozygous778808028
1264102091264102092GA57GENIChomozygous778808029
1264102112264102113TC57GENIChomozygous778808030
1264102373264102374GA55GENIChomozygous778808031
1264102418264102419TC61GENIChomozygous778808032
1264102632264102633CT51GENICpossibly homozygous778808033
1264103104264103105GA55GENIChomozygous778808034
1264103285264103286AG52GENIChomozygous778808035
1264103682264103683CT44GENIChomozygous778808036
1264104414264104415GA61GENIChomozygous778808037
1264105443264105444AC58INTERGENICpossibly homozygous778808038