chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2180897701180897702TC11GENIChomozygous110155209
2180898649180898650CT21GENIChomozygous110155210
2180900227180900228CG12GENIChomozygous110155211
2180900594180900595GA18GENIChomozygous110155212
2180901749180901750CT12GENIChomozygous110155213
2180901794180901795G12GENIChomozygous127711724
2180899506180899506A14GENIChomozygous127711721
2180900518180900518AA12GENIChomozygous127711722
2180901789180901791AA12GENIChomozygous127711723
2180901798180901799A12GENIChomozygous127711725
2180901803180901805GG12GENIChomozygous127711726
2180901813180901814C11GENIChomozygous127711727
2180901820180901821G10GENIChomozygous127711728
2180901840180901841G12GENIChomozygous127711729
2180901846180901847C11GENIChomozygous127711730
2180901868180901868T13GENIChomozygous127711731
2180901872180901873A13GENIChomozygous127711732
2180906629180906630AC21GENIChomozygous110155214
2180907151180907152TC16GENIChomozygous110155215
2180910701180910702AC19GENIChomozygous110155217
2180911479180911480TC14GENIChomozygous110155218
2180911912180911913TC27GENIChomozygous110155219
2180912556180912557AG22GENIChomozygous110155220
2180901886180901887AT13GENIChomozygous127825803
2180901883180901883GTA12GENIChomozygous127711733
2180901885180901885TT13GENIChomozygous127711734
2180901890180901890T14GENIChomozygous127711735
2180901891180901891AT14GENIChomozygous127711736