chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162479721824797219CA49GENICpossibly homozygous111764512
162479745524797456GT69GENICpossibly homozygous111764514
162479865724798658A11GENICpossibly homozygous129344216
162480006324800064CT46GENIChomozygous111764516
162480059924800604GCACA54GENIChomozygous129344217
162480076424800765GC51GENIChomozygous111764518
162480116024801161TG59GENIChomozygous111764520
162480139224801396TCTG56GENIChomozygous129344218
162480207824802079AG63GENIChomozygous111764522
162480231324802314GA47GENIChomozygous111764524
162480438524804386AG42GENIChomozygous111764526
162480463124804632T41GENIChomozygous129344219
162480476724804768GT49GENIChomozygous111764528
162480514724805148AG53GENIChomozygous111764530
162480572324805724CT52GENIChomozygous111764532