chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171851075618510757TC30GENIChomozygous110978285
171851087418510875AT31GENIChomozygous110978286
171851087518510876TC30GENIChomozygous110978288
171851108118511082TG25GENIChomozygous110978290
171851157218511573AC18GENIChomozygous110978292
171851208118512082AG20GENIChomozygous111175576
171851213518512136TG21GENIChomozygous110978294
171851225218512253TC20GENIChomozygous110978296
171851229518512296GA20GENIChomozygous110978298
171851242618512427GC13GENIChomozygous110978300
171851258218512583TC35GENIChomozygous110978302
171851267818512679AG22GENIChomozygous110978304
171851284418512845CT23GENIChomozygous110978306
171851313318513134GT18GENIChomozygous110978308
171851325918513260CT35GENIChomozygous110978310
171851343118513432CT34GENIChomozygous110978312
171851364718513648CT37GENIChomozygous110978314
171851364918513650GA39GENIChomozygous110978316
171851365418513655AG38GENIChomozygous110978318
171851371018513711AC42GENIChomozygous110978320
171851375718513758GT31GENIChomozygous110978322
171851402018514021AT37GENIChomozygous110978324
171851406618514067CT20GENIChomozygous110978326