chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2180897701180897702TC79GENICpossibly homozygous779241469
2180898649180898650CT51GENIChomozygous779241470
2180900227180900228CG72GENIChomozygous779241471
2180900594180900595GA81GENIChomozygous779241472
2180901749180901750CT47GENIChomozygous779241473
2180906629180906630AC70GENIChomozygous779241474
2180907151180907152TC87GENIChomozygous779241475
2180910079180910080TC24GENIChomozygous779241476
2180910701180910702AC47GENIChomozygous779241477
2180911479180911480TC60GENIChomozygous779241478
2180911912180911913TC63GENIChomozygous779241479
2180912556180912557AG81GENIChomozygous779241480