chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2180897701180897702TC30GENIChomozygous110155209
2180898649180898650CT23GENIChomozygous110155210
2180900227180900228CG46GENIChomozygous110155211
2180900594180900595GA30GENIChomozygous110155212
2180901749180901750CT41GENIChomozygous110155213
2180906629180906630AC9GENIChomozygous110155214
2180907151180907152TC23GENIChomozygous110155215
2180910079180910080TC17GENICpossibly homozygous110155216
2180910701180910702AC39GENIChomozygous110155217
2180911479180911480TC65GENIChomozygous110155218
2180911912180911913TC28GENIChomozygous110155219
2180912556180912557AG27GENIChomozygous110155220