chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157045106157045107AG19GENIChomozygous119413515
4157048245157048246GA36GENIChomozygous119413516
4157049467157049468TC12GENIChomozygous112905304
4157049524157049525GA7GENIChomozygous113062799
4157059168157059169CT18GENIChomozygous119317311
4157050983157050984AC24GENIChomozygous119317308
4157053551157053552CT27GENIChomozygous119317309
4157056615157056616GA34GENIChomozygous119317310
4157064842157064843AG22GENIChomozygous112905334
4157070459157070460TG27GENIChomozygous112905351
4157070792157070793GT20GENIChomozygous112905354
4157070924157070925TA32GENIChomozygous112905358
4157072044157072045GA29GENIChomozygous119317312
4157072963157072964GA18GENIChomozygous112905370
4157074372157074373GA40GENIChomozygous119317313
4157075126157075127GT17GENIChomozygous119413517
4157075180157075181AG23GENIChomozygous112905378
4157076809157076810GA22GENIChomozygous119317314
4157077047157077048CG26GENIChomozygous113247101
4157077443157077444CT21GENIChomozygous113247103