chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403243814032439AG15INTERGENIChomozygous68878195
101403309514033096AC11INTERGENIChomozygous68878199
101403319614033197TC14INTERGENIChomozygous68323344
101403360314033604GA6INTERGENICheterozygous68878202
101403470814034709TG10INTERGENICpossibly homozygous68878205
101403510314035104TA10INTERGENICpossibly homozygous68323346
101403577814035779CT13INTERGENIChomozygous68878208
101403580514035806CT17INTERGENIChomozygous68878210
101403582214035823CT17INTERGENIChomozygous68878213
101403605714036058AT22INTERGENIChomozygous69928891
101403612514036126AG14INTERGENIChomozygous68878216
101403612814036129TC13INTERGENIChomozygous68878219
101403640814036409CG13INTERGENIChomozygous68323350
101403992314039924GA9INTERGENIChomozygous68878223
101404109014041091TA8INTERGENIChomozygous68878226
101404128514041286AG11INTERGENICheterozygous68323378
101403674914036750CT10INTERGENIChomozygous69989912