chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403243814032439AG32INTERGENIChomozygous68878195
101403309514033096AC25INTERGENICpossibly homozygous68878199
101403319614033197TC36INTERGENIChomozygous68323344
101403360314033604GA41INTERGENIChomozygous68878202
101403470814034709TG10INTERGENICheterozygous68878205
101403510314035104TA31INTERGENIChomozygous68323346
101403577814035779CT29INTERGENIChomozygous68878208
101403580514035806CT29INTERGENIChomozygous68878210
101403582214035823CT28INTERGENIChomozygous68878213
101403612514036126AG30INTERGENIChomozygous68878216
101403612814036129TC30INTERGENIChomozygous68878219
101403640814036409CG27INTERGENIChomozygous68323350
101403674914036750CT34INTERGENICheterozygous69989912
101403992314039924GA24INTERGENIChomozygous68878223
101404109014041091TA27INTERGENICpossibly homozygous68878226
101404128514041286AG26INTERGENICheterozygous68323378
101403605714036058AT48INTERGENICpossibly homozygous69928891