chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141099160141099161CA39GENIChomozygous108260084
1141101140141101141CT25GENIChomozygous109049089
1141101245141101246AC25GENIChomozygous108260086
1141102193141102194CA5GENIChomozygous108260088
1141102413141102414AC32GENIChomozygous108260090
1141102613141102614TG28GENICheterozygous108936395
1141103349141103350AT22GENIChomozygous109049090
1141103797141103798AG45GENICheterozygous108260094
1141104298141104299TC32GENIChomozygous108260096
1141104542141104543AG24GENIChomozygous108260098
1141104681141104682CT26GENIChomozygous108936396
1141106799141106800CT14GENICpossibly homozygous109049091
1141108119141108120CT21GENIChomozygous108260106
1141109107141109108GA20GENIChomozygous109049092
1141109425141109426GA25GENIChomozygous109049093
1141110859141110860CT20GENIChomozygous109049094