chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185796818957968190TG10GENIChomozygous110474982
185796856557968566CT9GENIChomozygous110656246
185797338457973385TC14GENIChomozygous110474995
185797355157973552AG21GENIChomozygous110474997
185797357457973575TC15GENIChomozygous110656247
185797365957973660GT21GENIChomozygous110656248
185797367557973676CT18GENIChomozygous110656249
185797370857973709GT18GENIChomozygous110656250
185797372257973723TC15GENIChomozygous110656251
185797423457974235AG10GENIChomozygous110656252
185797423557974236AG10GENIChomozygous110656253
185797444557974446AC21GENIChomozygous110656254
185797448657974487CA7GENIChomozygous110656255
185797454057974541CT12GENIChomozygous110656256
185797454857974549CT12GENIChomozygous110656257
185797458357974584CG8GENIChomozygous110656258
185797459057974591GA10GENIChomozygous110656259
185797489657974897AT4GENIChomozygous110656260
185797600557976006TC18GENIChomozygous110656261
185797756357977564AT13GENIChomozygous110656262
185797778557977786CT19GENIChomozygous110656263
185797813757978138AG16GENIChomozygous110656264
185797941957979420AG19GENICpossibly homozygous110656265
185798035857980359GA9GENIChomozygous110656266
185798041057980411TG14GENICheterozygous110475006
185798194457981945AG9GENIChomozygous110475012
185798197657981977AT21GENIChomozygous110475014
185798053257980533GA3GENICheterozygous125390888